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Conjunctivitis
Wikipedia
Classification D ICD - 10 : H10 ICD - 9-CM : 372.0 MeSH : D003231 DiseasesDB : 3067 External resources MedlinePlus : 001010 eMedicine : emerg/110 Patient UK : Conjunctivitis v t e Diseases of the human eye Adnexa Eyelid Inflammation Stye Chalazion Blepharitis Entropion Ectropion Lagophthalmos Blepharochalasis Ptosis Blepharophimosis Xanthelasma Ankyloblepharon Eyelash Trichiasis Madarosis Lacrimal apparatus Dacryoadenitis Epiphora Dacryocystitis Xerophthalmia Orbit Exophthalmos Enophthalmos Orbital cellulitis Orbital lymphoma Periorbital cellulitis Conjunctiva Conjunctivitis allergic Pterygium Pseudopterygium Pinguecula Subconjunctival hemorrhage Globe Fibrous tunic Sclera Scleritis Episcleritis Cornea Keratitis herpetic acanthamoebic fungal Exposure Photokeratitis Corneal ulcer Thygeson's superficial punctate keratopathy Corneal dystrophy Fuchs' Meesmann Corneal ectasia Keratoconus Pellucid marginal degeneration Keratoglobus Terrien's marginal degeneration Post-LASIK ectasia Keratoconjunctivitis sicca Corneal opacity Corneal neovascularization Kayser–Fleischer ring Haab's striae Arcus senilis Band keratopathy Vascular tunic Iris Ciliary body Uveitis Intermediate uveitis Hyphema Rubeosis iridis Persistent pupillary membrane Iridodialysis Synechia Choroid Choroideremia Choroiditis Chorioretinitis Lens Cataract Congenital cataract Childhood cataract Aphakia Ectopia lentis Retina Retinitis Chorioretinitis Cytomegalovirus retinitis Retinal detachment Retinoschisis Ocular ischemic syndrome / Central retinal vein occlusion Central retinal artery occlusion Branch retinal artery occlusion Retinopathy diabetic hypertensive Purtscher's of prematurity Bietti's crystalline dystrophy Coats' disease Sickle cell Macular degeneration Retinitis pigmentosa Retinal haemorrhage Central serous retinopathy Macular edema Epiretinal membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary juvenile glaucoma Floater Leber's hereditary optic neuropathy Red eye Globe rupture Keratomycosis Phthisis bulbi Persistent fetal vasculature / Persistent hyperplastic primary vitreous Persistent tunica vasculosa lentis Familial exudative vitreoretinopathy Pathways Optic nerve Optic disc Optic neuritis optic papillitis Papilledema Foster Kennedy syndrome Optic atrophy Optic disc drusen Optic neuropathy Ischemic anterior (AION) posterior (PION) Kjer's Leber's hereditary Toxic and nutritional Strabismus Extraocular muscles Binocular vision Accommodation Paralytic strabismus Ophthalmoparesis Chronic progressive external ophthalmoplegia Kearns–Sayre syndrome palsies Oculomotor (III) Fourth-nerve (IV) Sixth-nerve (VI) Other strabismus Esotropia / Exotropia Hypertropia Heterophoria Esophoria Exophoria Cyclotropia Brown's syndrome Duane syndrome Other binocular Conjugate gaze palsy Convergence insufficiency Internuclear ophthalmoplegia One and a half syndrome Refraction Refractive error Hyperopia Myopia Astigmatism Anisometropia / Aniseikonia Presbyopia Vision disorders Blindness Amblyopia Leber's congenital amaurosis Diplopia Scotoma Color blindness Achromatopsia Dichromacy Monochromacy Nyctalopia Oguchi disease Blindness / Vision loss / Visual impairment Anopsia Hemianopsia binasal bitemporal homonymous Quadrantanopia subjective Asthenopia Hemeralopia Photophobia Scintillating scotoma Pupil Anisocoria Argyll Robertson pupil Marcus Gunn pupil Adie syndrome Miosis Mydriasis Cycloplegia Parinaud's syndrome Other Nystagmus Childhood blindness Infections Trachoma Onchocerciasis Authority control NDL : 00565682MMP2, PTAFR, PSMB9, LRRC8A, FERMT1, SAMD9, MMP1, MBTPS2, PIK3R1, PLG, POLH, PSMB4, PSMB8, RAG1, RAG2, ICOS, BLNK, TCF3, TNFRSF13B, GJB6, TNFRSF1A, UROS, WAS, WIPF1, XPA, XPC, TP63, STX16, SLC39A4, NLRC4, ERCC6, BTD, BTK, CD19, CD79A, CD79B, LRBA, COL7A1, CR2, DDB2, DKC1, DNASE1L3, USB1, ERCC2, ERF, FGFR2, FOXC2, GNAS, HLA-B, TNFRSF13C, IGHM, IGLL1, NLRP3, IKZF1, MBL3P, PLD3, IMMP1L, IGF2BP1, AD11, HM13, ALB, AOC3, IMPA1, CD14, GYPA, IFNGR1, IL4, CXCL8, IL10, IL12B, IL13, LGALS1, TYR, MBL2, PCOS1, ALK, CCL17, SOD3, STAT6, TEK, TNF, ERVK-19
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Oral Candidiasis
Wikipedia
Classification of oral candidiasis. [2] Primary oral candidiasis (group I) Pseudomembranous (acute or chronic) Erythematous (acute or chronic) Hyperplastic: plaque-like, nodular Candida-associated lesions: Denture related stomatitis, angular stomatitis, median rhomboid glossitis, linear gingival erythema Secondary oral candidiasis (group II) Oral manifestations of systemic mucocutaneous candidiasis (due to diseases such as thymic aplasia and candidiasis endocrinopathy syndrome) Oral candidiasis is a mycosis (fungal infection). ... The global human immunodeficiency virus / acquired immunodeficiency syndrome (HIV/AIDS) pandemic has been an important factor in the move away from the traditional classification since it has led to the formation of a new group of patients who present with atypical forms of oral candidiasis. [2] By appearance [ edit ] Three main clinical appearances of candidiasis are generally recognized: pseudomembranous, erythematous (atrophic) and hyperplastic. [4] Most often, affected individuals display one clear type or another, but sometimes there can be more than one clinical variant in the same person. [5] Pseudomembranous candidiasis in the mouth and oropharynx . ... Smoking is a known risk factor. [13] Chronic mucocutaneous candidiasis [ edit ] Main article: Chronic mucocutaneous candidiasis This refers to a group of rare syndromes characterized by chronic candidal lesions on the skin, in the mouth and on other mucous membranes (i.e., a secondary oral candidiasis). These include Localized chronic mucocutaneous candidiasis, diffuse mucocutaneous candidiasis (Candida granuloma), candidiasis–endocrinopathy syndrome and candidiasis thymoma syndrome. ... Oral candidiasis is sometimes presented in this manner as a symptom of a widely prevalent systemic candidiasis , candida hypersensitivity syndrome , yeast allergy , or gastrointestinal candida overgrowth , which are medically unrecognized conditions.LTF, IL17A, APCS, SH2D1A, SOD1, TNF, PSAP, DEFB4B, DEFB4A, IGFALS, PTPRH, IL22, IL12RB1, CXCL8, IL6, LRRCC1, ERVK-19, ERVK-9, ELK3, ERVK-24, ERVK-25, ERVK-18, ERVK-21, ERVK-10, SCLT1, ELK4, ERVK-8, HTN3, ERVK-7, STAT3, ZMYND10, TRAF3IP2, AKR1A1, NR4A3, IL23A, PLB1, ADH1A, STAT2, IFNG, ALS3, B2M, CBS, SEPTIN7, CDR1, CDR2, DEFB1, FLG, IL1A, CCL5, IL1B, IL1RN, IL4, LYZ, CYTB, ALB, PLCG1, PLD1, MUC1
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Hypothyroidism
Wikipedia
Numerous symptoms and signs are associated with hypothyroidism and can be related to the underlying cause, or a direct effect of having not enough thyroid hormones. [13] [14] Hashimoto's thyroiditis may present with the mass effect of a goiter (enlarged thyroid gland). [13] Symptoms and signs of hypothyroidism [13] Symptoms [13] Signs [13] Fatigue Dry, coarse skin Feeling cold Cool extremities Poor memory and concentration Myxedema ( mucopolysaccharide deposits in the skin) Constipation , dyspepsia [15] Hair loss Weight gain with poor appetite Slow pulse rate Shortness of breath Swelling of the limbs Hoarse voice Delayed relaxation of tendon reflexes In females, heavy menstrual periods (and later light periods ) Carpal tunnel syndrome Abnormal sensation Pleural effusion , ascites , pericardial effusion Poor hearing Delayed relaxation after testing the ankle jerk reflex is a characteristic sign of hypothyroidism and is associated with the severity of the hormone deficit. [7] Myxedema coma [ edit ] Man with myxedema or severe hypothyroidism showing an expressionless face, puffiness around the eyes and pallor Additional symptoms include swelling of the arms and legs and ascites. ... It is characterized by infiltration of the thyroid gland with T lymphocytes and autoantibodies against specific thyroid antigens such as thyroid peroxidase , thyroglobulin and the TSH receptor . [7] After women give birth, about 5% develop postpartum thyroiditis which can occur up to nine months afterwards. [26] This is characterized by a short period of hyperthyroidism followed by a period of hypothyroidism; 20–40% remain permanently hypothyroid. [26] Autoimmune thyroiditis is associated with other immune-mediated diseases such as diabetes mellitus type 1 , pernicious anemia , myasthenia gravis , celiac disease , rheumatoid arthritis and systemic lupus erythematosus . [7] It may occur as part of autoimmune polyendocrine syndrome ( type 1 and type 2 ). [7] Group Causes Primary hypothyroidism [7] Iodine deficiency (developing countries), autoimmune thyroiditis, subacute granulomatous thyroiditis , subacute lymphocytic thyroiditis , postpartum thyroiditis , previous thyroidectomy , acute infectious thyroiditis , [27] previous radioiodine treatment, previous external beam radiotherapy to the neck Medication: lithium -based mood stabilizers , amiodarone , interferon alpha , tyrosine kinase inhibitors such as sunitinib Central hypothyroidism [9] Lesions compressing the pituitary ( pituitary adenoma , craniopharyngioma , meningioma , glioma , Rathke's cleft cyst , metastasis , empty sella , aneurysm of the internal carotid artery ), surgery or radiation to the pituitary, drugs, injury, vascular disorders ( pituitary apoplexy , Sheehan syndrome , subarachnoid hemorrhage ), autoimmune diseases ( lymphocytic hypophysitis , polyglandular disorders), infiltrative diseases (iron overload due to hemochromatosis or thalassemia , neurosarcoidosis , Langerhans cell histiocytosis ), particular inherited congenital disorders, and infections ( tuberculosis , mycoses , syphilis ) Congenital hypothyroidism [28] Thyroid dysgenesis (75%), thyroid dyshormonogenesis (20%), maternal antibody or radioiodine transfer Syndromes: mutations (in GNAS complex locus , PAX8 , TTF-1/NKX2-1 , TTF-2/FOXE1 ), Pendred's syndrome (associated with sensorineural hearing loss ) Transiently: due to maternal iodine deficiency or excess, anti-TSH receptor antibodies, certain congenital disorders, neonatal illness Central: pituitary dysfunction (idiopathic, septo-optic dysplasia , deficiency of PIT1 , isolated TSH deficiency) In consumptive hypothyroidism, high levels of type 3 deiodinase inactivate thyroid hormones and thus lead to hypothyroidism. [29] High levels of type 3 deiodinase generally occur as the result of a hemangioma . [29] The condition is very rare. [29] Pathophysiology [ edit ] Diagram of the hypothalamic–pituitary–thyroid axis. ... The risk is higher in those with antibodies against thyroid peroxidase. [7] [37] Subclinical hypothyroidism is estimated to affect approximately 2% of children; in adults, subclinical hypothyroidism is more common in the elderly, and in Caucasians . [36] There is a much higher rate of thyroid disorders, the most common of which is hypothyroidism, in individuals with Down syndrome [21] [49] and Turner syndrome . [21] Very severe hypothyroidism and myxedema coma are rare, with it estimated to occur in 0.22 per million people a year. [16] The majority of cases occur in women over 60 years of age, although it may happen in all age groups. [16] Most hypothyroidism is primary in nature. ... "Consumptive Hypothyroidism: Case Report of Hepatic Hemangioendotheliomas Successfully Treated with Vincristine and Systematic Review of the Syndrome" . European Thyroid Journal . 6 (6): 321–327. doi : 10.1159/000481253 . ... "Health and disease in adults with Down syndrome" . Tidsskrift for den Norske Laegeforening (Review). 133 (3): 290–4. doi : 10.4045/tidsskr.12.0390 .TSHB, TRHR, TG, APOE, SLC30A10, SHH, KDM5C, TRH, IGF1, NR1D1, BDNF, NCOR1, ATP2A2, UCP2, NOS3, PNPLA3, SERPINA7, SOD1, UCP3, TOMM70, NCAM1, IL10, PCNA, CYP19A1, ADRB2, DCX, ALAD, GPX1, PAX8, CDK5R1, DPYSL2, MTHFR, ND3, ELAVL4, TSHR, GSN, CAV1, F7, NCOA1, TPO, ENTPD1, SLC34A1, MT3, WNT3A, APOA5, COL1A2, COL2A1, SLC2A1, SLC9A1, PLOD3, LIPC, PHKA1, SLC26A5, MAP1B, MSTN, MAP1A, OTOF, GIP, RELN, NKX2-1, NEFL, ARSA, NGF, AQP3, APOC3, NRGN, ANXA5, ANXA2, ANXA1, PLOD2, PLOD1, PAM, PCSK1, PITX2, GRK3, IGFBP2, HSD3B1, NOS2, NEFH, BAD, THRA, SRD5A1, STAR, MYH6, MYH7, L1CAM, NEFM, ATP5PO, SLC5A5, SLC16A2, POU1F1, SLC26A4, FOXE1, DUOX2, IGSF1, PROP1, PIK3CA, FMR1, DUOXA2, IYD, GNAS, IFNG, FOXP3, ADA, HLA-DRB1, IL2RA, THRB, PDE8B, CHD7, STAT1, RET, HESX1, TNFRSF11B, COX2, IFIH1, LHX4, PTPN22, PDE10A, VAV3, CP, SCN4A, DCLRE1C, PTEN, PTCH1, PRL, ALG8, SRD5A3, RNASEH2B, ARID1B, PVT1, NAA25, SRY, TWNK, DCAF17, POLG, PMM2, IQCN, PTPN11, SOX3, RAB5B, PLEKHA1, SIX3, SKI, ATXN2, SBF1, SKIV2L, SALL1, BACH2, SAA1, RREB1, ACP5, PHRF1, ROBO1, RMRP, RFC2, LRRC8A, PRDM16, RAG2, RAG1, RAD51B, RAB5C, ALX4, NFKB1, STAT4, DNM1L, DEAF1, FBLN5, STK25, DLEU1, STUB1, TIMMDC1, SLC25A37, PLXNC1, RASGRP1, GNE, CEP57, SH2B3, TANK, PHF21A, DACT1, TRANK1, ELMO1, KEAP1, PIEZO1, ACAP1, RNASEH2A, CDON, CD226, RAI1, SAMHD1, PANX1, TBL2, PIK3R5, KAT6B, AGO2, TMEM131, GPR161, DLL1, EXOSC2, ADNP, POGZ, IQSEC2, MYH15, TREX1, POLG2, EFEMP2, RRM2B, NEK6, SEMA3E, TTC37, BTNL2, HIRA, ALMS1, ZIC2, XRCC4, FANCI, WFS1, CLIP2, STEAP3, UFD1, TYK2, TSC2, SEC24C, TSC1, TNFRSF1B, TGIF1, RAB20, WDR11, TF, TDGF1, HNF1B, TBX1, KCNAB2, BHLHE40, TP63, PHIP, PTRH2, GTF2IRD1, MPDU1, EIF2AK3, MED7, FADS2, SUFU, TRIP13, BUB3, SH2D2A, BAZ1B, UBASH3A, KYNU, FOXH1, SGPL1, MAGEL2, SLC66A1, CCN4, TNFRSF14, PIK3C2A, DNAH1, CLPB, GATA1, GABRD, ARL6IP6, FYN, FUCA1, FLT3, FLII, FOXI1, FGFR1, FGF8, MB21D2, EXT2, ELN, UBR1, DIO2, HIPK1, JMJD1C, SPATA13, GAS1, GCH1, CPT1C, HORMAD2, EDARADD, HPD, PROKR2, HNF4A, TANGO2, DNAJC19, NRG1, HBB, GTF2I, HT, KCTD19, GPC1, GP1BB, GNB1, ENPP1, GLI2, GH1, FGD2, FOXK1, NKX2-5, RSBN1L, LINC01301, ARVCF, MIR3681HG, PCAT1, ABCC6, IFNG-AS1, LINC01934, LINC00824, PTCSC2, CASC19, APC, SLC25A4, AKT1, LINC02357, LINC02621, ADCY7, ADAR, RERE, LINC00271, LINC01387, CD247, COMT, COL4A1, CDH13, LRBA, HECTD4, CD80, HCG22, CD2, MICOS10, LINC00299, CBLB, CAMK4, C12orf76, FMNL1, BUB1B, BUB1, HSD17B3, HJV, TRNS1, ITK, ARID5B, KARS1, KCNJ10, TRNQ, TRNN, MACIR, TRNL2, TRNL1, TRNH, KCNH7, LIFR, LIG4, LIMK1, TRNF, LPP, ND6, ND5, ND4, ND1, COX3, LRP4, PNPT1, COX1, DISP1, ITCH, MARS1, RNASEH2C, JAK1, MCM8, C1QTNF6, IGHGP, TRNS2, IL12RB2, IL7R, NPHS1, PLVAP, IL2RG, IP6K3, INPP5B, INSR, TRIM8, NODAL, NFATC1, IRF4, IRF5, TRNW, OPA1, LEP, MED12, TNF, CTLA4, CD274, CAT, ALB, PDCD1, DIO3, GPT, SLC20A1, MAPK3, PTH, THRA1/BTR, POMC, PIK3CG, PIK3CD, PIK3CB, ACHE, LDLR, SHBG, IL6, IGFBP3, MIR224, GLUL, FSHR, LHX3, PLA2G2A, BRAF, LPA, CST3, BCL2, KCNQ1, GCG, TTF1, GHRHR, NR1I3, GJA1, REN, HLA-DQB1, AGT, PPIG, CRP, SLCO1C1, BRD2, CD68, ACTB, MOK, DECR1, MTTP, ANGPTL3, HAMP, SCGB3A2, SLC2A8, APOBR, GPR151, SLCO6A1, ANTXR2, AMN, COASY, ANGPTL8, USE1, COQ9, SLC16A10, GSTO2, CAMKMT, GSTK1, PCSK9, MAGI3, COPD, TIGIT, NUDT10, GLIS3, DACT2, SLC2A12, SERPINA13P, EHMT1, MIR206, UBE2Z, DNAJC17, IL33, MLXIPL, GSTT2B, POTEF, ZGLP1, CXADRP1, RORA, SMUG1, DPP4, GLP1R, GFAP, XRCC6, FASN, EGR1, EFNA5, DNMT1, LAMP1, DNASE2, DMP1, DIO1, ACE, CYP2B6, CXADR, GPER1, GSTP1, GSTT1, GZMB, HLA-C, HLA-DQA1, HOXD13, HPT, IGFBP1, IGHD, IGHG3, IL2, IL4, IL17A, CXCL10, ISG20, KRT6A, CTNNB1, MAPK14, CRH, BAAT, AGER, JAG1, AHR, APOA1, APOB, APP, AQP4, AR, ARNTL, ARR3, ATM, ATP4A, ATP7B, AVP, BCL6, CNR1, HCN2, BMPR2, C2, CAD, CALM1, CALM2, CALM3, CAPZB, CASP3, CASR, KRIT1, CD28, CD36, CETP, KRT17, LGALS3, SLC39A14, VEGFA, PER2, NR1I2, KSR1, ABCB11, CNBP, XK, TNFSF4, LRP1, TTN, TGFB1, TFAM, TERT, TEF, TRB, HSPB3, ADIPOQ, NCOR2, MED13, KCNE2, MPZL2, TRIM13, NCOA2, TXNRD2, TSBP1, PPARGC1A, RAB40B, METAP2, NLRP1, DKK1, SIRT1, TRAM1, SYT1, STAT3, SST, PPARD, LRPAP1, MAP2, MBL2, MME, MPO, MT1B, CLDN11, PAEP, PDE3B, ATP8B1, PIK3C3, PLIN1, PON1, PPARA, PPARG, SREBF2, PRKAA1, PRKAA2, PRKAB1, PRKAR1A, DNAJC3, PTGS2, PTH1R, RARA, RBP4, SLC2A3, SLC13A1, SOD2, SPG7, SREBF1, MTCO2P12
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Muscle–eye–brain Disease
Wikipedia
MEB is phenotypically similar to the Walker–Warburg syndrome (WWS), both disorders are congenital muscular dystrophy. ... "Muscle, Eye and Brain Disease: A New Syndrome". Neuropediatrics . 8 (S 01): 553. doi : 10.1055/s-0028-1091594 . ... "Muscle–Eye–Brain Disease; a Rare Form of Syndromic Congenital Muscular Dystrophy" . ... "Ophthalmological Findings in a New Syndrome with Muscle, Eye and Brain Involvement". ... "Response to Santavuori et al. regarding Walker–Warburg syndrome and muscle–eye–brain disease".
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Premenstrual Dysphoric Disorder
Wikipedia
PMID 16417420 . ^ Biggs, WS; Demuth, RH (October 2011). "Premenstrual syndrome and premenstrual dysphoric disorder". ... S2CID 2048753 . ^ Condon, John T (April 1993). "The Premenstrual Syndrome: A Twin Study". The British Journal of Psychiatry . ... PMID 21427640 . ^ a b "Premenstrual Syndrome, Management (Green-top Guideline No. 48)" . ... "New perspectives on the treatment of premenstrual syndrome and premenstrual dysphoric disorder". ... "Cognitive-behavioral and pharmacological interventions for premenstrual syndrome or premenstrual dysphoric disorder: a meta-analysis".
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Seborrhoeic Dermatitis
Wikipedia
., that seen in polycystic ovary syndrome ). [26] [27] In addition, seborrhoea, as well as acne , are commonly associated with puberty due to the steep increase of androgen levels at that time. [28] In accordance with the involvement of androgens in seborrhoea, antiandrogens, such as cyproterone acetate , [29] spironolactone , [30] flutamide , [31] [32] and nilutamide , [33] [34] are highly effective in alleviating the condition. [26] [35] As such, they are used in the treatment of seborrhoea, [26] [35] particularly severe cases. [36] While beneficial in seborrhoea, effectiveness may vary with different antiandrogens; for instance, spironolactone (which is regarded as a relatively weak antiandrogen) has been found to produce a 50% improvement after three months of treatment, whereas flutamide has been found to result in an 80% improvement within three months. [26] [32] Cyproterone acetate is similarly more potent and effective than spironolactone, and results in considerable improvement or disappearance of acne and seborrhoea in 90% of patients within three months. [37] Systemic antiandrogen therapy are generally used to treat seborrhoea only in women, and not in men, as these medications can result in feminization (e.g., gynecomastia ), sexual dysfunction , and infertility in males. [38] [39] In addition, antiandrogens theoretically have the potential to feminize male fetuses in pregnant women, and for this reason, are usually combined with effective birth control in sexually active women who can or may become pregnant. [37] Antihistamines [ edit ] Antihistamines are used primarily to reduce itching , if present. ... Diagnosis and Management of Polycystic Ovary Syndrome . Springer Science & Business Media. pp. 240–. ... American Academy of Dermatology: Seborrheic dermatitis v t e Diseases of the skin and appendages by morphology Growths Epidermal Wart Callus Seborrheic keratosis Acrochordon Molluscum contagiosum Actinic keratosis Squamous-cell carcinoma Basal-cell carcinoma Merkel-cell carcinoma Nevus sebaceous Trichoepithelioma Pigmented Freckles Lentigo Melasma Nevus Melanoma Dermal and subcutaneous Epidermal inclusion cyst Hemangioma Dermatofibroma (benign fibrous histiocytoma) Keloid Lipoma Neurofibroma Xanthoma Kaposi's sarcoma Infantile digital fibromatosis Granular cell tumor Leiomyoma Lymphangioma circumscriptum Myxoid cyst Rashes With epidermal involvement Eczematous Contact dermatitis Atopic dermatitis Seborrheic dermatitis Stasis dermatitis Lichen simplex chronicus Darier's disease Glucagonoma syndrome Langerhans cell histiocytosis Lichen sclerosus Pemphigus foliaceus Wiskott–Aldrich syndrome Zinc deficiency Scaling Psoriasis Tinea ( Corporis Cruris Pedis Manuum Faciei ) Pityriasis rosea Secondary syphilis Mycosis fungoides Systemic lupus erythematosus Pityriasis rubra pilaris Parapsoriasis Ichthyosis Blistering Herpes simplex Herpes zoster Varicella Bullous impetigo Acute contact dermatitis Pemphigus vulgaris Bullous pemphigoid Dermatitis herpetiformis Porphyria cutanea tarda Epidermolysis bullosa simplex Papular Scabies Insect bite reactions Lichen planus Miliaria Keratosis pilaris Lichen spinulosus Transient acantholytic dermatosis Lichen nitidus Pityriasis lichenoides et varioliformis acuta Pustular Acne vulgaris Acne rosacea Folliculitis Impetigo Candidiasis Gonococcemia Dermatophyte Coccidioidomycosis Subcorneal pustular dermatosis Hypopigmented Tinea versicolor Vitiligo Pityriasis alba Postinflammatory hyperpigmentation Tuberous sclerosis Idiopathic guttate hypomelanosis Leprosy Hypopigmented mycosis fungoides Without epidermal involvement Red Blanchable Erythema Generalized Drug eruptions Viral exanthems Toxic erythema Systemic lupus erythematosus Localized Cellulitis Abscess Boil Erythema nodosum Carcinoid syndrome Fixed drug eruption Specialized Urticaria Erythema ( Multiforme Migrans Gyratum repens Annulare centrifugum Ab igne ) Nonblanchable Purpura Macular Thrombocytopenic purpura Actinic/solar purpura Papular Disseminated intravascular coagulation Vasculitis Indurated Scleroderma / morphea Granuloma annulare Lichen sclerosis et atrophicus Necrobiosis lipoidica Miscellaneous disorders Ulcers Hair Telogen effluvium Androgenic alopecia Alopecia areata Systemic lupus erythematosus Tinea capitis Loose anagen syndrome Lichen planopilaris Folliculitis decalvans Acne keloidalis nuchae Nail Onychomycosis Psoriasis Paronychia Ingrown nail Mucous membrane Aphthous stomatitis Oral candidiasis Lichen planus Leukoplakia Pemphigus vulgaris Mucous membrane pemphigoid Cicatricial pemphigoid Herpesvirus Coxsackievirus Syphilis Systemic histoplasmosis Squamous-cell carcinoma v t e Dermatitis and eczema Atopic dermatitis Besnier's prurigo Seborrheic dermatitis Pityriasis simplex capillitii Cradle cap Contact dermatitis ( allergic , irritant ) plants: Urushiol-induced contact dermatitis African blackwood dermatitis Tulip fingers other: Abietic acid dermatitis Diaper rash Airbag dermatitis Baboon syndrome Contact stomatitis Protein contact dermatitis Eczema Autoimmune estrogen dermatitis Autoimmune progesterone dermatitis Breast eczema Ear eczema Eyelid dermatitis Topical steroid addiction Hand eczema Chronic vesiculobullous hand eczema Hyperkeratotic hand dermatitis Autosensitization dermatitis / Id reaction Candidid Dermatophytid Molluscum dermatitis Circumostomy eczema Dyshidrosis Juvenile plantar dermatosis Nummular eczema Nutritional deficiency eczema Sulzberger–Garbe syndrome Xerotic eczema Pruritus / Itch / Prurigo Lichen simplex chronicus / Prurigo nodularis by location: Pruritus ani Pruritus scroti Pruritus vulvae Scalp pruritus Drug-induced pruritus Hydroxyethyl starch-induced pruritus Senile pruritus Aquagenic pruritus Aquadynia Adult blaschkitis due to liver disease Biliary pruritus Cholestatic pruritus Prion pruritus Prurigo pigmentosa Prurigo simplex Puncta pruritica Uremic pruritus Other substances taken internally: Bromoderma Fixed drug reaction Nummular dermatitis Pityriasis alba Papuloerythroderma of Ofuji v t e Other dermatological preparations ( D11 ) Anti-seborrheics Antiandrogens Bicalutamide Cyproterone acetate Flutamide Spironolactone Antifungals Bifonazole Cetrimonium bromide ( cetrimide ) Ciclopirox olamine (ciclopirox) Climbazole Clotrimazole Ketoconazole Miconazole Piroctone olamine Selenium disulfide (selenium sulfide) Xenysalate Zinc pyrithione (pyrithione zinc) Antihistamines Calcineurin inhibitors Cyclosporin Pimecrolimus Tacrolimus Isotretinoin Keratolytics Coal tar Resorcinol Salicylic acid Sulfur Urea ( urea-containing cream ) Lithium salts Lithium gluconate Lithium succinate Topical corticosteroids (e.g., hydrocortisone ) Skin lightening Hydroquinone Mequinol Monobenzone Skin darkening Afamelanotide Melanotan II Anti-inflammatories Oxaceprol Gamolenic acid Pimecrolimus Tacrolimus Alitretinoin Topical corticosteroids (e.g., hydrocortisone ) Alopecia treatments 5α-Reductase inhibitors Alfatradiol Dutasteride Finasteride Saw palmetto extract Antiandrogens Bicalutamide Cyproterone acetate Flutamide Spironolactone Topilutamide (fluridil) Potassium channel openers Minoxidil Others Nepidermin Hair growth inhibitors 5α-Reductase inhibitors Dutasteride Finasteride Antiandrogens Bicalutamide Cyproterone acetate Flutamide Spironolactone Eflornithine Others Androgens (e.g., testosterone ) Brimonidine Calcium gluconate Estrogens (e.g., estradiol ) Hyaluronic acid Magnesium sulfate Pregnenolone acetate Progestogens (e.g., progesterone ) Povidone-iodine Tiratricol Medicine portal
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Urinary Incontinence
Wikipedia
Urge urinary incontinence, is caused by uninhibited contractions of the detrusor muscle , a condition known as overactive bladder syndrome . It is characterized by leaking of large amounts of urine in association with insufficient warning to get to the bathroom in time. ... Neurogenic disorders like multiple sclerosis , spina bifida , Parkinson's disease , strokes and spinal cord injury can all interfere with nerve function of the bladder. [17] This can lead to neurogenic bladder dysfunction Overactive bladder syndrome . However, the etiology behind this is usually different between men and women, as mentioned above. ... This incontinence is associated with sudden forceful contractions of the detrusor muscle (bladder muscle), leading to an intense feeling of urination, and incontinence if the person does not reach the bathroom on time. The syndrome is known as overactive bladder syndrome , and it's related to dysfunction of the detrusor muscle. [20] Children [ edit ] Voiding dysfunction Main article: Enuresis Urination, or voiding, is a complex activity. ... Urge incontinence is an involuntary loss of urine occurring while suddenly feeling the need or urge to urinate, usually secondary to overactive bladder syndrome . Overflow incontinence is the incontinence that happens suddenly without feeling an urge to urinate and without necessarily doing any physical activities. It is also known as under-active bladder syndrome. This usually happens with chronic obstruction of the bladder outlet or with diseases damaging the nerves supplying the urinary bladder.ADRA1A, MAPK1, IL1RAPL1, CNKSR2, DKK1, IQSEC2, ADNP, ATP13A2, ZFYVE26, FTSJ1, SUFU, ATXN10, CHMP2B, TOR1AIP1, SACS, COQ2, FLVCR1, ATL1, MID2, VCP, SLC9A6, COG5, ZNF41, USP7, USP9X, JRK, PEX11B, CACNA1H, CACNA1G, CYP7B1, ARHGEF6, FRMPD4, LRIG2, WASHC5, AP5Z1, MED12, STUB1, FARS2, RETREG1, BNC2, IFT57, ASXL3, VANGL1, C19orf12, SLC9A7, HS6ST2, TIMM50, RAB39B, NIPA1, CPT1C, HGSNAT, PTCHD1, ARX, NEXMIF, ZNF81, USP27X, SPG11, FUZ, PANK2, GBA2, PRDM8, GJC2, VANGL2, GATAD2B, HACE1, ALS2, TRPV4, ALG13, HPSE2, CXorf56, IRF2BPL, MTMR14, UPF3B, FA2H, ZNF711, ATXN8, MYF6, HEXB, NF2, NAGLU, BIN1, MECP2, KIF5A, KCND3, KCNC3, IGHMBP2, ARSA, HSPD1, HMBS, HLA-DRB1, HLA-DQB1, MNX1, HCFC1, CLCNKB, GRIN2B, GDI1, GBE1, GABRG2, GABRB3, GABRA1, FMR1, ACSL4, DNMT1, DNM2, DMD, DLG3, AUH, ADGRB2, ABCD1, NOTCH3, PAK3, PDCD1, TYROBP, TTR, TRIO, TSPAN7, AGTR2, TBP, TBCD, TBXT, SYP, SPG7, SPAST, SMARCB1, SLC20A2, SLC16A2, SLC12A3, SLC2A1, SGSH, CCL2, SCN9A, SCN8A, ATXN8OS, RYR1, RTN2, RPS6KA3, ALDH18A1, PSAP, HTRA1, PDGFRB, PDGFB, CLCN4, VIP, COL1A1, COL3A1, DCN, HTR2A, VIPR1, NPY, TGFB1, A2M
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Spinocerebellar Ataxia Type 7
Gene_reviews
Lower motor neuron involvement (fasciculations, weakness w/muscle wasting, areflexia, distal sensory loss) Sensory loss 40% ↓ sensation to light touch, pinprick, &/or joint position Restless leg syndrome 35% Discomfort in legs resulting in uncontrollable urge to move one’s legs, typically worse in evening or nighttime Cognitive decline 20% Impaired executive function Behavior disorder/ Psychosis 10% Altered mentation Impaired reality testing Cone-rod dystrophy 70% Loss of central vision & color vision Abnormal fundoscopic exam Neurologic findings. ... Disorders with Retinal Degeneration in the Differential Diagnosis of Spinocerebellar Ataxia Type 7 View in own window Gene(s) Disorder MOI Eye Findings Neurologic & Pathologic Findings Distinguishing Features CRX Cone-rod dystrophy 2 (OMIM 120970) AD Impaired color vision; central scotoma No neurologic findings No neurologic findings MT-ND1 MT-ND4 MT-ND6 1 Leber hereditary optic neuropathy Mat Impaired color vision; central scotoma No neurologic findings Usually midlife presentation OPA3 Costeff syndrome (3-methylglutaconic aciduria type 3) AR Bilateral optic atrophy Chorea, spastic paraparesis, mild ataxia Optic atrophy in childhood (age <10 yrs) Common in persons of Iraqi Jewish origin due to founder variant WFS1 CISD2 Wolfram syndrome (See WFS1 Wolfram Syndrome Spectrum Disorder.) ... Bladder function History of spastic bladder symptoms: urgency, frequency, difficulty voiding Referral to urologist Consider urodynamic eval. Restless legs syndrome Obtain comprehensive history w/emphasis on triggering & relieving factors. ... Cognitive/ Psychiatric Assess for cognitive dysfunction assoc w/cerebellar cognitive & affective syndrome (executive function, language processing, visuospatial / visuoconstructional skills, emotion regulation) Consider use of: CCAS scale 2 to evaluate cognitive & emotional involvement; Psychiatrist, psychologist, neuropsychologist if needed. ... Botulinum toxin injections should be reserved for severe or unresponsive bladder dysfunction. Restless legs syndrome Pharmacologic treatment Levodopa or dopamine agonist Chronic pain Requires specialist eval & management Refer to pain clinic or pain specialist.ATXN7, ATXN1, ATXN2, CACNA1A, RUBCN, PPP2R2B, PRKCG, CWF19L1, ANO10, WWOX, SNX14, MME, TDP2, SPTBN2, CIC, TRPC3, AFG3L2, NOP56, STUB1, SCYL1, CACNA1G, FOXC1, VWA3B, ELOVL5, UBA5, CCDC88C, RBM17, TGM6, TTBK2, ATXN1L, SYT14, GRM1, GRID2, GFI1, ATXN3, LY6E, SUMO2, KAT2A, RELN, TPP1, CASP7, NOX1, DNAJB1P1, SMG1, PCP2, CTCF, PRPF8, SPTLC3, APLP2, TAF2, ATG12, HDAC3, CASP3, CRX, CTSD, DPYSL3, ATN1, GUCA1A, HTT, DNAJA1, HSPA4, DNAJB1, IFNB1, ENPP2, PDYN, PML, PRNP, RNF4, RPE65, ATXN8OS, SLC1A3, TBP, TP53, SUMO1, TRRAP, ULK1, SUPT3H, SCAANT1
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Astigmatism
Wikipedia
Astigmatism at Curlie v t e Diseases of the human eye Adnexa Eyelid Inflammation Stye Chalazion Blepharitis Entropion Ectropion Lagophthalmos Blepharochalasis Ptosis Blepharophimosis Xanthelasma Ankyloblepharon Eyelash Trichiasis Madarosis Lacrimal apparatus Dacryoadenitis Epiphora Dacryocystitis Xerophthalmia Orbit Exophthalmos Enophthalmos Orbital cellulitis Orbital lymphoma Periorbital cellulitis Conjunctiva Conjunctivitis allergic Pterygium Pseudopterygium Pinguecula Subconjunctival hemorrhage Globe Fibrous tunic Sclera Scleritis Episcleritis Cornea Keratitis herpetic acanthamoebic fungal Exposure Photokeratitis Corneal ulcer Thygeson's superficial punctate keratopathy Corneal dystrophy Fuchs' Meesmann Corneal ectasia Keratoconus Pellucid marginal degeneration Keratoglobus Terrien's marginal degeneration Post-LASIK ectasia Keratoconjunctivitis sicca Corneal opacity Corneal neovascularization Kayser–Fleischer ring Haab's striae Arcus senilis Band keratopathy Vascular tunic Iris Ciliary body Uveitis Intermediate uveitis Hyphema Rubeosis iridis Persistent pupillary membrane Iridodialysis Synechia Choroid Choroideremia Choroiditis Chorioretinitis Lens Cataract Congenital cataract Childhood cataract Aphakia Ectopia lentis Retina Retinitis Chorioretinitis Cytomegalovirus retinitis Retinal detachment Retinoschisis Ocular ischemic syndrome / Central retinal vein occlusion Central retinal artery occlusion Branch retinal artery occlusion Retinopathy diabetic hypertensive Purtscher's of prematurity Bietti's crystalline dystrophy Coats' disease Sickle cell Macular degeneration Retinitis pigmentosa Retinal haemorrhage Central serous retinopathy Macular edema Epiretinal membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary juvenile glaucoma Floater Leber's hereditary optic neuropathy Red eye Globe rupture Keratomycosis Phthisis bulbi Persistent fetal vasculature / Persistent hyperplastic primary vitreous Persistent tunica vasculosa lentis Familial exudative vitreoretinopathy Pathways Optic nerve Optic disc Optic neuritis optic papillitis Papilledema Foster Kennedy syndrome Optic atrophy Optic disc drusen Optic neuropathy Ischemic anterior (AION) posterior (PION) Kjer's Leber's hereditary Toxic and nutritional Strabismus Extraocular muscles Binocular vision Accommodation Paralytic strabismus Ophthalmoparesis Chronic progressive external ophthalmoplegia Kearns–Sayre syndrome palsies Oculomotor (III) Fourth-nerve (IV) Sixth-nerve (VI) Other strabismus Esotropia / Exotropia Hypertropia Heterophoria Esophoria Exophoria Cyclotropia Brown's syndrome Duane syndrome Other binocular Conjugate gaze palsy Convergence insufficiency Internuclear ophthalmoplegia One and a half syndrome Refraction Refractive error Hyperopia Myopia Astigmatism Anisometropia / Aniseikonia Presbyopia Vision disorders Blindness Amblyopia Leber's congenital amaurosis Diplopia Scotoma Color blindness Achromatopsia Dichromacy Monochromacy Nyctalopia Oguchi disease Blindness / Vision loss / Visual impairment Anopsia Hemianopsia binasal bitemporal homonymous Quadrantanopia subjective Asthenopia Hemeralopia Photophobia Scintillating scotoma Pupil Anisocoria Argyll Robertson pupil Marcus Gunn pupil Adie syndrome Miosis Mydriasis Cycloplegia Parinaud's syndrome Other Nystagmus Childhood blindness Infections Trachoma Onchocerciasis Authority control NDL : 00569289 Medicine portalTYR, CASC15, CACNA1F, ARCN1, PRRX2, ANKRD11, SLC25A24, VSX1, SMARCAL1, WAC, MBTPS2, P4HTM, PRMT7, TRAF3IP1, PHIP, FANCL, RFWD3, SETD5, UBE2T, NIPBL, AUTS2, NPLOC4, VAX2, ADNP, PACS2, POGZ, EMC1, ARSG, KDM5B, CLDN16, MAD2L2, ECEL1, ARHGEF2, AP3D1, CDK13, FANCI, MBD5, RNF113A, CHRDL1, PROX1-AS1, RNU4ATAC, MIR184, GTF2H5, BLOC1S3, ZDHHC24, EBF3, LVRN, KCNV2, SPATA5, CLDN19, MPLKIP, DNAJC21, SGSM1, UBE3B, MFF, LOXL3, SLX4, CHD6, CEP78, BRIP1, TRIM8, PALB2, CCDC28B, SLC39A8, PIEZO2, FANCM, CC2D2A, KIDINS220, ARID1B, USP9X, HERC2, XRCC2, ERCC4, H3-3A, VARS1, GTF2E2, GRIN2B, GNAQ, GLRB, FBN1, FANCG, FANCF, FANCB, FANCE, FANCD2, FANCC, FANCA, ERCC3, MAG, ERCC2, EGFR, DPYD, DNAH5, COL11A1, COL9A3, COL9A2, COL9A1, CHD4, CHD3, C1QBP, BRCA2, BRCA1, BBS1, HARS1, H1-4, MECP2, CHMP1A, CLRN1, TUB, TEAD1, TCF4, TBCE, RAD51C, RAD51, PTPN11, PDGFRA, PCYT1A, LINC02422, TRNS2, TRIM37, NEUROD2, GPR143, NFIX, MFT2, TNMD, CYLD, CCT, MT1L, OCA2, TWIST1, THOP1, ART1, LINC00273, MELTF, ATR, TYMS, TMTC3, TGFB2, STAR, SFPQ, FTMT, CCL21, IGFBP7, CREBZF, PLXNA2, PYCARD, APH1A, CCL1
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Dystonia
Wikipedia
The combination of blepharospasmodic contractions and oromandibular dystonia is called cranial dystonia or Meige's syndrome . Segmental dystonias [ edit ] Segmental dystonias affect two adjoining parts of the body: [ citation needed ] Hemidystonia affects an arm and foot on one side of the body. ... It may become difficult to find a comfortable position for arms and legs with even the minor exertions associated with holding arms crossed causing significant pain similar to restless leg syndrome . Affected persons may notice trembling in the diaphragm while breathing, or the need to place hands in pockets, under legs while sitting or under pillows while sleeping to keep them still and to reduce pain. ... Sufferers may be diagnosed as having similar and perhaps related disorders including Parkinson's disease , essential tremor , carpal tunnel syndrome , temporomandibular joint disorder , Tourette's syndrome , conversion disorder or other neuromuscular movement disorders. ... Then, dystonia were reported in detail in 1911, when Hermann Oppenheim , [43] Edward Flatau and Wladyslaw Sterling described some Jewish children affected by a syndrome that was retrospectively considered to represent familial cases of DYT1 dystonia. ... During the following years it became evident that dystonia syndromes are numerous and diversified, new terminological descriptors (e.g., dystonia plus, heredodegenerative dystonias, etc.) and additional classification schemes were introduced.KMT2B, GNAL, THAP1, PRKRA, TOR1A, GLRA1, ALDH5A1, ATCAY, PENK, ATP2B4, LRP2, PANK2, TH, GCH1, SGCE, MCF2L, TUBB4A, ATP1A3, TAF1, DST, CACNA1A, PLA2G6, ND6, HPCA, PRKN, ATXN3, ATXN1, TIMM8A, DRD2, ANO3, BDNF, SLC30A10, LY6E, NIF3L1, ATXN2, ARX, ADCY5, ADAR, ATP13A2, HSPA8, LRRC7, SLC2A1, SLC6A3, COL6A3, ANPEP, TRAF3, TOR1AIP1, CIZ1, PRRT2, NELFE, SCN8A, FA2H, DPEP1, DNAJC12, GCDH, ATXN7, DYT7, ALS2, ABCB6, PDE10A, TBP, TOR1B, BCAP31, COQ8A, WDR45, ARSG, SLC39A14, SUCLA2, ACTB, POLG, HLA-DQB1, ATM, POTEF, TPP1, TOR1AIP2, DRD1, LRRK2, COX20, GRM5, SERAC1, MECP2, PINK1, HIBCH, DYT17, SMUG1, TBC1D24, SLC12A5, COA6, DYT15, KLHL14, FBXO7, TSEN54, KCNT1, PNKD, NDUFAF6, SLC39A8, VAC14, ZNF415, SCNM1, PANK1, CYP2U1, GCNA, SAR1A, C19orf12, APTX, SLC19A3, NUBPL, ATAD3A, ZC4H2, DCAF17, KCTD17, NMS, TFDP1, CAMTA2, GABRA1, HSPA4, HPD, HLA-B, HCFC1, GSN, GPI, GLB1, GDF10, GAD1, GABRG2, GABRB3, EMD, SETX, EEF1A2, ECHS1, DRD5, DNTT, DBT, DBH, CRH, CASP3, CACNA1B, ATP7B, APOE, HSPA5, KCND3, KCNJ6, COX2, ARFGEF2, TUBB3, SCO2, POLR1C, ZFYVE9, SQSTM1, RGS9, ZNF142, HSP90B2P, NKX2-1, ACY1, SLC20A2, SLC18A2, SLC6A8, SCP2, RBBP6, PSEN1, PDHA1, PDE2A, OPRM1, NDUFA9, ND3, ND1, DYT23
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Multifocal Lymphangioendotheliomatosis
Wikipedia
ISBN 0-7216-2921-0 . v t e Tumours of blood vessels Blood vessel Hemangiosarcoma Blue rubber bleb nevus syndrome Hemangioendothelioma Composite Endovascular papillary Epithelioid Kaposiform Infantile Retiform ) Spindle cell Proliferating angioendotheliomatosis Hemangiopericytoma Venous lake Kaposi's sarcoma African cutaneous African lymphadenopathic AIDS-associated Classic Immunosuppression-associated Hemangioblastoma Hemangioma Capillary Cavernous Glomeruloid Microvenular Targeted hemosiderotic Angioma Cherry Seriginosum Spider Tufted Universal angiomatosis Angiokeratoma of Mibelli Angiolipoma Pyogenic granuloma Lymphatic Lymphangioma / lymphangiosarcoma Lymphangioma circumscriptum Acquired progressive lymphangioma PEComa Lymphangioleiomyomatosis Cystic hygroma Multifocal lymphangioendotheliomatosis Lymphangiomatosis Either Angioma / angiosarcoma Angiofibroma This Dermal and subcutaneous growths article is a stub .
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Pterygium Colli, Isolated
Omim
Graham and Smith (1981) described an 11-week old infant evaluated for possible XO Turner syndrome because of pterygium colli. She also showed low posterior hair line, protruding ears with an uplifted lower pinna bilaterally, loose facial skin, epicanthal folds, and a short nose.
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Hyperlipidemia, Familial Combined, 2
Omim
Patients with FCHL are at increased risk of cardiovascular disease and mortality and have a high frequency of comorbidity with other metabolic conditions such as type 2 diabetes, nonalcoholic fatty liver disease, steatohepatitis, and the metabolic syndrome (summary by Bello-Chavolla et al., 2018).
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Rhizomelic Dysplasia, Scoliosis, And Retinitis Pigmentosa
Omim
Megarbane et al. (2006) distinguished the disorder in this family from other syndromes with skeletal dysplasia and eye abnormalities.
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Migraine With Or Without Aura, Susceptibility To, 10
Omim
For a phenotypic description and discussion of genetic heterogeneity of migraine headaches, see MGR1 (157300). Mapping Since migraine is a syndrome instead of a clearly differentiated disease, Anttila et al. (2006) hypothesized that individual clinical components of migraine (i.e., traits such as pulsating pain and photophobia, among others) might represent reflections of specific rather than shared loci and thus independently contribute to susceptibility to migraine.
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Follicular Atrophoderma, Perioral Pigmented, With Milia And Epidermoid Cysts
Omim
The patients' manifestations resembled those of Bazex-Dupre-Christol syndrome (BZX; 301845), but BZX is an X-linked disorder, has a different distribution of follicular atrophoderma, and has basal cell carcinoma and hypotrichosis as features.
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Deafness, Conductive, With Malformed External Ear
Omim
The authors noted similarities to the patients previously described by Mengel et al. (1969) and Cantu et al. (1978), but in light of the differences exhibited by their patients (microcephaly and facial abnormalities), they speculated that the latter might represent a new syndrome. Inheritance Consanguinity and affected sibs suggest autosomal recessive inheritance of this disorder (Mengel et al., 1969).
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Neutrophil Migration
Omim
Although random mobility was normal, chemotaxis of leukocytes from the patients and their fathers was deficient. (In the 'lazy leukocyte syndrome' (150550), random movement is also defective.)
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Angiofibroma
Wikipedia
External links [ edit ] Classification D ICD - 10 : D10.6 ( ILDS D23.L75) ICD-O : M9160/0 MeSH : D018322 DiseasesDB : 32229 v t e Tumours of blood vessels Blood vessel Hemangiosarcoma Blue rubber bleb nevus syndrome Hemangioendothelioma Composite Endovascular papillary Epithelioid Kaposiform Infantile Retiform ) Spindle cell Proliferating angioendotheliomatosis Hemangiopericytoma Venous lake Kaposi's sarcoma African cutaneous African lymphadenopathic AIDS-associated Classic Immunosuppression-associated Hemangioblastoma Hemangioma Capillary Cavernous Glomeruloid Microvenular Targeted hemosiderotic Angioma Cherry Seriginosum Spider Tufted Universal angiomatosis Angiokeratoma of Mibelli Angiolipoma Pyogenic granuloma Lymphatic Lymphangioma / lymphangiosarcoma Lymphangioma circumscriptum Acquired progressive lymphangioma PEComa Lymphangioleiomyomatosis Cystic hygroma Multifocal lymphangioendotheliomatosis Lymphangiomatosis Either Angioma / angiosarcoma Angiofibroma This Dermal and subcutaneous growths article is a stub .
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Papular Mucinosis Of Infancy
Wikipedia
ISBN 978-1-4160-2999-1 . v t e Mucinosis / Lichen myxedematosus Localized lichen myxedematosus Discrete papular lichen myxedematosus Acral persistent papular mucinosis Self-healing papular mucinosis / Self-healing juvenile cutaneous mucinosis Papular mucinosis of infancy Atypical lichen myxedematosus Atypical tuberous myxedema Nodular lichen myxedematosus Other primary mucinoses Cutaneous focal mucinosis Cutaneous lupus mucinosis Eccrine mucinosis Alopecia mucinosa Perifollicular mucinosis Stiff skin syndrome Generalized lichen myxedematosus Secondary mucinoses Basal-cell carcinoma Granuloma annulare This cutaneous condition article is a stub .