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Psoriasis-Related Juvenile Idiopathic Arthritis
Orphanet
Specific examples include ankylosing spondylitis, reactive arthritis, inflamatory bowel disease, Behçet disease, Kawasaki disease, sarcoidosis, Blau syndrome, systemic lupus erythematosus, Sweet syndrome, and some infections such as Lyme or Whipple disease.ACP3, MTSS1, KAT6B, STAB1, TTLL5, AVL9, UHRF1BP1L, TNIK, R3HDM2, PACSIN2, BTG3, FAXDC2, WASF3, PLK2, RHOBTB1, FCHSD2, UBE3C, TNFAIP8, PCYT1B, B4GALT5, KLF4, CD83, TNFRSF10C, MAD1L1, H2BC8, DYSF, NR4A3, CXCR4, RNF103, UBE2E1, TUBB2A, TNFAIP6, MAFF, SIPA1L1, TFPI, MIR22HG, LILRA5, TREML1, NEAT1, JMJD1C, C9orf72, APOBEC3A, ZFC3H1, CAMSAP1, RASGEF1B, SIK1, CMTM2, BEND2, ANKRD9, SLC22A16, AOPEP, FOXP1, ACRBP, MAML2, C2orf88, SH3BGRL2, NDEL1, HERPUD2, ZFAND3, ETNK1, FAM20A, RBM47, WWOX, MS4A4A, MEX3C, ASAP1, ADCY7, THBS1, TFDP1, HBEGF, GNG11, GMPR, FOSL2, FOSB, FOS, FCGR1A, ETV6, CTTN, ELF2, EGR1, EGF, DUSP4, DUSP2, DUSP1, DDIT3, CXCL1, GADD45A, DAPK1, CTLA4, CREM, CLU, CD14, CD8B, CALD1, C8B, BTG1, RERE, AREG, AQP9, ALOX12, TCF7L2, GP1BB, H2AC8, NRG1, STIM1, STAT3, SLC11A1, SLC2A3, PROS1, MAPK1, PLOD2, PLAUR, PGM5, PER1, OSM, OLR1, NR4A2, MSN, ITGA2B, JUN, HSPA6, IGF1R, IL1RN, CXCR2, ITGB5, MYZAP, KCNJ15, KRAS, LPP, SMAD3, MAP2, IL23R, MEFV, ERAP1, DDR1, HLA-DRB1, TNF, MBL2
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Eyelid Dermatitis
Wikipedia
. ^ https://www.medicalnewstoday.com/articles/321004#complications ^ https://www.medicalnewstoday.com/articles/321004#types-and-causes ^ https://onlinelibrary.wiley.com/doi/full/10.1111/j.1600-0536.2006.00927.x ^ https://www.dermnetnz.org/topics/eyelid-contact-dermatitis/ ^ https://journals.lww.com/dermatitis/Abstract/2007/06000/Common_Contact_Allergens_Associated_with_Eyelid.3.aspx ^ https://www.mayoclinic.org/diseases-conditions/contact-dermatitis/symptoms-causes/syc-20352742 ^ https://pubmed.ncbi.nlm.nih.gov/18346395/ ^ https://www.healthline.com/health/eyelid-dermatitis 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 This cutaneous condition article is a stub .
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Asthenozoospermia
Wikipedia
External links [ edit ] GP Notebook Fertility network v t e Male diseases of the pelvis and genitals Internal Testicular Orchitis Hydrocele testis Testicular cancer Testicular torsion Male infertility Aspermia Asthenozoospermia Azoospermia Hyperspermia Hypospermia Oligospermia Necrospermia Teratospermia Epididymis Epididymitis Spermatocele Hematocele Prostate Prostatitis Acute prostatitis Chronic bacterial prostatitis Chronic prostatitis/chronic pelvic pain syndrome Asymptomatic inflammatory prostatitis Benign prostatic hyperplasia Prostate cancer Seminal vesicle Seminal vesiculitis External Penis Balanoposthitis / Balanitis Balanitis plasmacellularis Pseudoepitheliomatous keratotic and micaceous balanitis Phimosis Paraphimosis Priapism Sexual dysfunction Erectile dysfunction Peyronie's disease Penile cancer Penile fracture Balanitis xerotica obliterans Other Hematospermia Retrograde ejaculation Postorgasmic illness syndrome This article related to the genitourinary system is a stub .
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Supernumerary Body Part
Wikipedia
A supernumerary phantom limb is the sensation of having an extra limb or body part despite no such limb actually existing. It is an uncommon syndrome, usually due to some kind of brain injuries in the somatosensory cortex or in some parts of the right hemisphere of the brain, usually due to a stroke in the brain. ... Accessed 10 July 2006. ^ PatientPlus. " Cervical ribs and thoracic outlet syndrome ". Accessed 10 July 2006. ^ Grumbach, M.M., Conte, F.A., 1998.
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Columnaris
Wikipedia
Columnaris disease v t e Fish diseases and parasites Pathogens Aeromonas salmonicida Nervous necrosis virus Columnaris Enteric redmouth Fin rot Fish dropsy Flavobacterium Hematopoietic necrosis Heterosigma akashiwo Hole in the head Hypodermal and hematopoietic necrosis Infectious pancreatic necrosis Koi herpes virus Mycobacterium marinum Novirhabdovirus Pfiesteria piscicida Photobacterium damselae ssp piscicida Salmon anemia Streptococcus iniae Spring viraemia of carp Taura syndrome UDN VHS White spot Yellowhead Parasites Abergasilus Amoebic gill disease Anisakis Carp lice Ceratomyxa shasta Clinostomum marginatum Dactylogyrus vastator Diphyllobothrium Cymothoa exigua Eustrongylidosis Epizootic ulcerative syndrome Flukes Glugea Gyrodactylus salaris Henneguya zschokkei Ich (freshwater) Ich (marine) Kudoa thyrsites Lernaeocera branchialis Microsporidia Monogenea Myxobolus cerebralis Myxosporea Nanophyetus salmincola Pseudorhabdosynochus spp.
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Compensatory Hyperhidrosis
Wikipedia
The difference in temperatures between the sympathetically under- and overactive regions can be as high as 10 Celsius. [ citation needed ] Contents 1 Variations 2 Mechanism 3 Epidemiology 4 References Variations [ edit ] Gustatory sweating or Frey's syndrome is another presentation of autonomic neuropathy . [3] Gustatory sweating is brought on while eating, thinking or talking about food that produces a strong salivary stimulus. ... Surg . 81 (3): 1043–7. doi : 10.1016/j.athoracsur.2005.09.044 . PMID 16488719 . ^ Frey's syndrome at Who Named It? ^ Disorders of Sweating: Hyperhidrosis [ permanent dead link ] ^ "טיפול בהזעת יתר" .
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Leukodystrophy, Hypomyelinating, 9
Omim
At age 2 years, she did not fix or follow, had axial hypotonia with poor head control, some dystonic movements, and an extrapyramidal syndrome with increased reflexes. A low level of cognition and lack of visual contact in this patient were consistent with early severe atrophy present at brain imaging. ... INHERITANCE - Autosomal recessive HEAD & NECK Head - Microcephaly (1 patient) Eyes - Nystagmus - Poor smooth pursuit - Poor visual fixation (1 patient) MUSCLE, SOFT TISSUES - Hypertonicity of the lower limbs NEUROLOGIC Central Nervous System - Delayed psychomotor development - Mental retardation, mild to severe - Spasticity, more apparent in the lower limbs - Ataxia - Dysmetria - Dysarthria - Extrapyramidal syndrome - Poor or absent independent walking - Hyperreflexia - Intention tremor - Brain imaging shows hypomyelination - Thin corpus callosum - Global cerebral atrophy, mild (in some patients) - Epilepsy, focal occipital (in 1 patient) MISCELLANEOUS - Onset in the first year of life - Variable severity - Six patients from 5 families have been reported (last curated November 2018) MOLECULAR BASIS - Caused by mutation in the arginyl-tRNA synthetase 1 gene (RARS1, 107820.0001 ) ▲ Close
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Acalvaria
Wikipedia
PMID 8362912 . v t e Congenital malformations and deformations of nervous system Brain Neural tube defect Anencephaly Acephaly Acrania Acalvaria Iniencephaly Encephalocele Chiari malformation Other Microcephaly Congenital hydrocephalus Dandy–Walker syndrome other reduction deformities Holoprosencephaly Lissencephaly Microlissencephaly Pachygyria Hydranencephaly Septo-optic dysplasia Megalencephaly Hemimegalencephaly CNS cyst Porencephaly Schizencephaly Polymicrogyria Bilateral frontoparietal polymicrogyria Spinal cord Neural tube defect Spina bifida Rachischisis Other Currarino syndrome Diastomatomyelia Syringomyelia
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Vaginal Hypoplasia
Wikipedia
Diagnostically, it may look similar to a vaginal obstruction such as can be caused by an imperforate hymen or, less commonly, a transverse vaginal septum . [ citation needed ] It is frequently associated with Mayer-Rokitansky-Küstner-Hauser (MRKH) syndrome, in which the most common result is an absent uterus in conjunction with a deformed or missing vagina, despite the presence of normal ovaries and normal external genitalia. ... In this case prompt medical action is required. [ citation needed ] Causes [ edit ] The main causes are Müllerian agenesis and complete androgen insensitivity syndrome . [1] Treatment [ edit ] Inflatable vaginal expander ZSI 200 NS ZSI 200 NS vaginal expander stretching the female vagina In order to facilitate sexual intercourse , the main treatments are self-dilation methods (using intra-vaginal cylinders or inflatable expanders (vaginal stents) of increasing size) and surgical vaginoplasty to lengthen the vagina. [1] Self-dilation has a high success rate, estimated at 75%, and is usually the first-line treatment due to low surgical invasiveness . [1] Overall, the complication rates are significantly lower with dilation than with vaginoplasty. [1] Surgery is indicated when there is inability or reluctance to perform self-dilation, or where it is performed but with failed result.
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Hydroa Vacciniforme
Wikipedia
In contrast out of 11 severe patients in this study, 6 had evidence of chronic EBV infection, 5 had hypersensitivity to mosquito bites, 4 had virus-associated hemophagocytic syndrome . 6 of the severe group had natural killer-cell lymphocytosis in the peripheral blood. [6] Diagnosis [ edit ] Histology of the affected area commonly shows dense perivascular lymphocytic infiltration with reticulated degeneration of the epidermis. ... External links [ edit ] Classification D ICD - 10 : L56.860 ( ILDS L56.860) ICD - 9-CM : 692.79 MeSH : D006837 DiseasesDB : 33843 External resources eMedicine : article/1119445 Orphanet : 330058 v t e Radiation-related disorders / Photodermatoses Ultraviolet / ionizing Sunburn Phytophotodermatitis Solar urticaria Polymorphous light eruption Benign summer light eruption Juvenile spring eruption Acne aestivalis Hydroa vacciniforme Solar erythema Non-ionizing Actinic rays Actinic keratosis Atrophic actinic keratosis Hyperkeratotic actinic keratosis Lichenoid actinic keratosis Pigmented actinic keratosis Actinic cheilitis Actinic granuloma Actinic prurigo Chronic actinic dermatitis Infrared / heat Erythema ab igne ( Kangri ulcer Kairo cancer Kang cancer Peat fire cancer ) Cutis rhomboidalis nuchae Poikiloderma of Civatte Other Radiation dermatitis Acute Chronic radiodermatitis ) Favre–Racouchot syndrome Photoaging Photosensitivity with HIV infection Phototoxic tar dermatitis
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Focal Nodular Hyperplasia
Wikipedia
Other patterns include telangiectatic, hyperplastic-adenomatous, and lesions with focal large-cell dysplasia. [2] Rarely, these lesions may be multiple or can occur as part of a syndrome with hemangiomas, epithelioid hemangioendothelioma, hepatic adenomas, fibrolamellar hepatocellular carcinoma, vascular malformations of the brain, meningiomas, and/or astrocytomas. [2] Pathophysiology [ edit ] FNH is not a true neoplasm; it is believed to result from localized hyperplastic hepatocyte response to an underlying congenital arteriovenous malformation. ... External links [ edit ] Classification D ICD - 10 : K76.8 MeSH : D020518 DiseasesDB : 33467 External resources eMedicine : radio/286 v t e Digestive system neoplasia GI tract Upper Esophagus Squamous cell carcinoma Adenocarcinoma Stomach Gastric carcinoma Signet ring cell carcinoma Gastric lymphoma MALT lymphoma Linitis plastica Lower Small intestine Duodenal cancer Adenocarcinoma Appendix Carcinoid Pseudomyxoma peritonei Colon/rectum Colorectal polyp : adenoma , hyperplastic , juvenile , sessile serrated adenoma , traditional serrated adenoma , Peutz–Jeghers Cronkhite–Canada Polyposis syndromes: Juvenile MUTYH-associated Familial adenomatous / Gardner's Polymerase proofreading-associated Serrated polyposis Neoplasm: Adenocarcinoma Familial adenomatous polyposis Hereditary nonpolyposis colorectal cancer Anus Squamous cell carcinoma Upper and/or lower Gastrointestinal stromal tumor Krukenberg tumor (metastatic) Accessory Liver malignant : Hepatocellular carcinoma Fibrolamellar Hepatoblastoma benign : Hepatocellular adenoma Cavernous hemangioma hyperplasia : Focal nodular hyperplasia Nodular regenerative hyperplasia Biliary tract bile duct : Cholangiocarcinoma Klatskin tumor gallbladder : Gallbladder cancer Pancreas exocrine pancreas : Adenocarcinoma Pancreatic ductal carcinoma cystic neoplasms : Serous microcystic adenoma Intraductal papillary mucinous neoplasm Mucinous cystic neoplasm Solid pseudopapillary neoplasm Pancreatoblastoma Peritoneum Primary peritoneal carcinoma Peritoneal mesothelioma Desmoplastic small round cell tumor
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Hematospermia
Wikipedia
External links [ edit ] Classification D ICD - 10 : N50.1 ICD - 9-CM : 608.82 MeSH : D051516 DiseasesDB : 31879 External resources eMedicine : med/3466 Patient UK : Hematospermia v t e Male diseases of the pelvis and genitals Internal Testicular Orchitis Hydrocele testis Testicular cancer Testicular torsion Male infertility Aspermia Asthenozoospermia Azoospermia Hyperspermia Hypospermia Oligospermia Necrospermia Teratospermia Epididymis Epididymitis Spermatocele Hematocele Prostate Prostatitis Acute prostatitis Chronic bacterial prostatitis Chronic prostatitis/chronic pelvic pain syndrome Asymptomatic inflammatory prostatitis Benign prostatic hyperplasia Prostate cancer Seminal vesicle Seminal vesiculitis External Penis Balanoposthitis / Balanitis Balanitis plasmacellularis Pseudoepitheliomatous keratotic and micaceous balanitis Phimosis Paraphimosis Priapism Sexual dysfunction Erectile dysfunction Peyronie's disease Penile cancer Penile fracture Balanitis xerotica obliterans Other Hematospermia Retrograde ejaculation Postorgasmic illness syndrome
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Neurogenic Shock
Wikipedia
External links [ edit ] Classification D ICD - 10 : R57.8 ICD - 9-CM : 785 MeSH : D012769 v t e Shock Distributive Septic shock Neurogenic shock Anaphylactic shock Toxic shock syndrome Obstructive Abdominal compartment syndrome Low volume Hemorrhage Hypovolemia Osmotic shock Other Spinal shock Cryptic shock Vasodilatory shock
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Crayfish Plague
Wikipedia
Global Invasive Species Database Canadian Fisheries and Oceans Crayfish Plague information Trade Environment Database Case Study on Crayfish Plague v t e Diseases of crustaceans Bitter crab disease Crayfish plague Gaffkaemia Infectious hypodermal and haematopoietic necrosis Necrotising hepatopancreatitis Paragonimiasis Taura syndrome White spot syndrome Yellowhead disease Taxon identifiers Wikidata : Q2858203 Wikispecies : Aphanomyces astaci EoL : 133454 EPPO : APHAAS Fungorum : 118727 GBIF : 3202936 GISD : 107 iNaturalist : 209110 IRMNG : 11247906 ISC : 93177 ITIS : 13861 NBN : BMSSYS0000001544 NCBI : 112090 WoRMS : 394837
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Congenital Heart Defects, Dysmorphic Facial Features, And Intellectual Developmental Disorder
Omim
Clinical Features Sifrim et al. (2016) reported 7 unrelated children, ranging in age from infancy to 12 years, with a syndrome associated with atrial and/or ventricular septal congenital heart defects. ... Six of the patients were ascertained from a cohort of 518 trios in which a child with syndromic congenital heart defects underwent exome sequencing; the seventh patient was 1 of 86 singleton cases.
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Sting-Associated Vasculopathy With Onset In Infancy
Wikipedia
. ^ Jeremiah N, Neven B, Gentili M, Callebaut I, Maschalidi S, Stolzenberg M-C, Goudin N, Fremond, M-L, Nitschke P, Molina TJ, Blanche S, Picard C, Rice GI, Crow YJ, Manel N, Fischer A, Bader-Meunier B, Rieux-Laucat, F (2014) Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations. ... Activated STING in a vascular and pulmonary syndrome. New Eng J Med 371: 507-518 ^ Miner, Jonathan J.; Yan, Nan; Platt, Derek J.; Wu, Jianjun; Gonugunta, Vijay K.; Sakai, Tomomi; Miner, Cathrine A.; Smith, Amber M.; Ai, Teresa L. (2017-11-06).
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Pancreatoblastoma
Wikipedia
. ^ http://www.orpha.net/data/patho/GB/uk-pancrea.pdf - External links [ edit ] Classification D ICD-O : M8971/3 MeSH : C537162 C537162, C537162 v t e Digestive system neoplasia GI tract Upper Esophagus Squamous cell carcinoma Adenocarcinoma Stomach Gastric carcinoma Signet ring cell carcinoma Gastric lymphoma MALT lymphoma Linitis plastica Lower Small intestine Duodenal cancer Adenocarcinoma Appendix Carcinoid Pseudomyxoma peritonei Colon/rectum Colorectal polyp : adenoma , hyperplastic , juvenile , sessile serrated adenoma , traditional serrated adenoma , Peutz–Jeghers Cronkhite–Canada Polyposis syndromes: Juvenile MUTYH-associated Familial adenomatous / Gardner's Polymerase proofreading-associated Serrated polyposis Neoplasm: Adenocarcinoma Familial adenomatous polyposis Hereditary nonpolyposis colorectal cancer Anus Squamous cell carcinoma Upper and/or lower Gastrointestinal stromal tumor Krukenberg tumor (metastatic) Accessory Liver malignant : Hepatocellular carcinoma Fibrolamellar Hepatoblastoma benign : Hepatocellular adenoma Cavernous hemangioma hyperplasia : Focal nodular hyperplasia Nodular regenerative hyperplasia Biliary tract bile duct : Cholangiocarcinoma Klatskin tumor gallbladder : Gallbladder cancer Pancreas exocrine pancreas : Adenocarcinoma Pancreatic ductal carcinoma cystic neoplasms : Serous microcystic adenoma Intraductal papillary mucinous neoplasm Mucinous cystic neoplasm Solid pseudopapillary neoplasm Pancreatoblastoma Peritoneum Primary peritoneal carcinoma Peritoneal mesothelioma Desmoplastic small round cell tumor v t e Connective / soft tissue tumors and sarcomas Not otherwise specified Soft-tissue sarcoma Desmoplastic small-round-cell tumor Connective tissue neoplasm Fibromatous Fibroma / fibrosarcoma : Dermatofibrosarcoma protuberans Desmoplastic fibroma Fibroma / fibromatosis : Aggressive infantile fibromatosis Aponeurotic fibroma Collagenous fibroma Diffuse infantile fibromatosis Familial myxovascular fibromas Fibroma of tendon sheath Fibromatosis colli Infantile digital fibromatosis Juvenile hyaline fibromatosis Plantar fibromatosis Pleomorphic fibroma Oral submucous fibrosis Histiocytoma / histiocytic sarcoma : Benign fibrous histiocytoma Malignant fibrous histiocytoma Atypical fibroxanthoma Solitary fibrous tumor Myxomatous Myxoma / myxosarcoma Cutaneous myxoma Superficial acral fibromyxoma Angiomyxoma Ossifying fibromyxoid tumour Fibroepithelial Brenner tumour Fibroadenoma Phyllodes tumor Synovial -like Synovial sarcoma Clear-cell sarcoma Lipomatous Lipoma / liposarcoma Myelolipoma Myxoid liposarcoma PEComa Angiomyolipoma Chondroid lipoma Intradermal spindle cell lipoma Pleomorphic lipoma Lipoblastomatosis Spindle cell lipoma Hibernoma Myomatous general: Myoma / myosarcoma smooth muscle : Leiomyoma / leiomyosarcoma skeletal muscle : Rhabdomyoma / rhabdomyosarcoma : Embryonal rhabdomyosarcoma Sarcoma botryoides Alveolar rhabdomyosarcoma Leiomyoma Angioleiomyoma Angiolipoleiomyoma Genital leiomyoma Leiomyosarcoma Multiple cutaneous and uterine leiomyomatosis syndrome Multiple cutaneous leiomyoma Neural fibrolipoma Solitary cutaneous leiomyoma STUMP Complex mixed and stromal Adenomyoma Pleomorphic adenoma Mixed Müllerian tumor Mesoblastic nephroma Wilms' tumor Malignant rhabdoid tumour Clear-cell sarcoma of the kidney Hepatoblastoma Pancreatoblastoma Carcinosarcoma Mesothelial Mesothelioma Adenomatoid tumor
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X-Linked Dystonia Parkinsonism
Wikipedia
Find sources: "X-linked dystonia parkinsonism" – news · newspapers · books · scholar · JSTOR ( December 2014 ) ( Learn how and when to remove this template message ) X-linked dystonia parkinsonism Other names Lubag syndrome This condition is inherited in an X-linked recessive manner Specialty Neurology X-linked dystonia parkinsonism (XDP) , also known as Lubag Syndrome or X-linked Dystonia of Panay, is a rare x-linked progressive movement disorder with high penetrance found almost exclusively in males from the Panay, Philippines . [1] It is characterized by dystonic movements first typically occurring in the 3rd and 4th decade of life.
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Hereditary Motor And Sensory Neuropathy V
Omim
Inheritance was autosomal dominant, and onset was usually in the first 2 decades of life with difficulty in walking. The syndrome superficially resembled HMSN types I and II (CMT1 and CMT2) with distal muscle wasting and weakness involving the legs more than the arms. ... The authors noted that whereas most patients presented coexistence of the 2 syndromes, 2 had predominant pyramidal signs, and 2 had a predominant sensory neuropathy.
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Cutaneous Amoebiasis
Wikipedia
External links [ edit ] Classification D ICD - 10 : A06.7 ICD - 9-CM : 006.6 v t e Amoebozoal diseases Lobosea ( free-living ) Centramoebida Acanthamoeba Acanthamoeba keratitis Cutaneous acanthamoebiasis Granulomatous amoebic encephalitis Acanthamoeba infection Balamuthia mandrillaris Balamuthia amoebic encephalitis Balamuthia infection Flabellinia Sappinia diploidea / Sappinia pedata Sappinia amoebic encephalitis Conosa / Archamoebae Entamoeba histolytica Amoebiasis Amoebic dysentery Amoebic liver abscess Cutaneous amoebiasis Amoebic brain abscess Amebiasis cutis Entamoeba gingivalis 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 This infection-related cutaneous condition article is a stub .