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Keratitis, Hereditary
Omim
There was no skin or mucous membrane involvement in patients with autosomal dominant keratitis, as has been shown to occur with keratitis in patients suffering from epidermolysis bullosa simplex (226670) by Granek and Baden (1980), in the EEC syndrome (129900) by Mawhorter et al. (1985), or the keratitis-ichthyosis-deafness syndrome (KID; 148210) by Wilson et al. (1991).
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Ear Pits, Posterior Helical
Omim
In addition, at least 2 cases of the Beckwith-Wiedemann syndrome (BWS; 130650) had occurred in this family. ... The proband's mother had Hermansky-Pudlak syndrome (see 203300); the authors noted that ear malformations are not known to be associated with that condition.
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Acropectorovertebral Dysplasia
Omim
Description Acropectorovertebral dysgenesis, or F syndrome, is an autosomal dominant skeletal dysplasia characterized by carpal and tarsal synostoses, syndactyly between the first and second fingers, hypodactyly and polydactyly of feet, and abnormalities of the sternum and spine (summary by Thiele et al., 2004). ... Mapping In a study of 9 affected and 18 unaffected individuals from 4 generations of the original family reported by Grosse et al. (1969), Thiele et al. (2004) mapped the F syndrome to a 6.5-cM region on chromosome 2q36 with a maximum lod score of 4.21 for marker D2S2250.
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Malignant Sex Cord Stromal Tumor Of Ovary
Orphanet
Malignant SCST of ovary is also found in association with enchondromatosis, Peutz Jeghers syndrome (see these terms) and Maffuci syndrome.
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Sympathetic Ophthalmia
Orphanet
Other diseases associated with granulomatous uveitis, including sarcoidosis and Vogt-Koyanagi-Harada syndrome (see these terms) or uveal effusion syndrome, may also be considered in the absence of a recognized history of ocular trauma.
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Progressive Non-Infectious Anterior Vertebral Fusion
Orphanet
PAVF can occur isolated or less frequently, as part of a syndrome. Syndrome associated manifestations include facial dysmorphism, absence of one cervical vertebrae, radio-ulnar synostosis, exostosis, generalized overgrowth, split cord malformation and/or situs inversus totalis (see this term).
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Ventricular Septal Defect 3
Omim
Large VSDs that go unrepaired may give rise to cardiac enlargement, congestive heart failure, pulmonary hypertension, Eisenmenger's syndrome, delayed fetal brain development, arrhythmias, and even sudden cardiac death (summary by Wang et al. (2011, 2011)). Other congenital cardiac defects caused by mutation in the NKX2-5 gene include atrial septal defect with or without atrioventricular conduction defects (ASD7; 108900), tetralogy of Fallot (see TOF, 187500), conotruncal malformations (see 217095), and hypoplastic left heart syndrome (HLHS2; 614435). For a discussion of genetic heterogeneity of ventricular septal defect, see VSD1 (614429).
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Arachnoiditis
Orphanet
It can also be caused by bacterial and viral spinal infections (7%) and repeated subarachnoid injections of anticancer drugs or antimetabolites. Syringomyelia, cauda equina syndrome, pseudomeningoceles, intrathecal cysts or tethering of the spinal cord and nerve roots (NR) may complicate lumbosacral arachnoiditis. ... Differential diagnosis Differential diagnoses include intra-spinal hematoma or dislodged disc fragment if the condition presents immediately after surgery, and Failed Back Surgery Syndrome (FBSS). Some patients are diagnosed with fibromyalgia (see this term), but these symptoms are likely to occur as a secondary feature due to the altered spinal dynamics.
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Congenital Muscular Dystrophy
Orphanet
The group includes myopathies with abnormalities at different cellular levels: the extracellular matrix (MDC1A, UCMD; see these terms), the dystrophin-associated glycoprotein complex (alphadystroglycanopathies, integrinopathies see these terms), the endoplasmic reticulum (rigid spine syndrome [RSMD1], and the nuclear envelope (LMNA-related CMD; [L-CMD] and Nesprin-1-related CMD; see these terms). ... Differential diagnosis Differential diagnoses include congenital and early onset neuromuscular disorders, mainly congenital myopathies, spinal muscular atrophy and congenital myasthenic syndromes (see these theses terms). Patients with mutations in genes identified in other neighbour muscular disorders such as congenital myopathies may present sometimes as a CMD (including the finding of dystrophic features on muscle biopsy) without specific ultrastructural abnormalities on muscle biopsy.LAMA2, FKTN, DMD, COL6A1, SELENON, FKRP, SGCA, DYSF, CAPN3, SGCG, ANO5, DAG1, SGCD, TTN, SGCB, TRIM32, PRIMA1, TCAP, BCHE, ACHE, DES, LMNA, PLEC, LDB3, TRIM63, CAV3, CAVIN1, TOR1AIP1, POMGNT1, POMT1, COL6A3, COL6A2, GMPPB, POMT2, LARGE1, BAG3, CHKB, B3GALNT2, DNAJB6, CRPPA, NR0B1, B4GAT1, LIMS2, POMGNT2, INPP5K, RXYLT1, BVES, SYNE2, SYNE1, TNPO3, BEST1, PSAT1, NEB, SIL1, PMM2, RYR1, HSPB8, PIEZO2, PHGDH, HNRNPA2B1, DOK7, RIF1, DPM1, BUB3, DPM3, TRIP13, TRIP4, POMK, CEP57, TMEM43, PNKP, PYROXD1, TTN-AS1, HNRNPA1, BUB1B, COL4A1, CRYAB, AHCY, MSTN, GK, COL12A1, BUB1, EMD, UTRN, SSPN, IGF1, TRIM72, MYOT, SMCHD1, FSHMD1A, LTBP4, DMPK, ANO1, MB, TRPV2, LRRC7, ANPEP, CCN2, TRAF3, HMGCR, FRG1, FLNC, FHL1, HSPA8, MYOF, STAT5A, SPP1, CHKA, SGCE, DTNA, ANXA6, ORAI1, FST, IL6, DUX4, TNFRSF11B, ACTB, KITLG, MIR21, JAG1, ITGA7, NR3C2, LIF, CUX1, MMD, DCN, MIR222, LARGE2, MIR29C, NAT9, MIR188, MIR146A, MIR130B, KIF7, SUN1, DLG4, MIR30C1, DPEP1, DUSP6, CELF1, B3GNT2, GJB6, CCR2, WWP1, MIR486-1, ACE, DNMT3B, DUSP10, DNAH8, MIR340, MIR30C2, ACTN3, HPGDS, ACVR2B, LAMA1, MUL1, HAMP, TRAPPC11, AQP4, AQP1, APRT, EGFLAM, TNFAIP8L2, TOR1A, ANXA2, SETD7, OBSCN, ANXA1, B4GALNT2, TPH2, KIDINS220, BGN, CMD1B, CD38, EFEMP2, PCSK9, TRAT1, SIDT2, ZCCHC17, PARP1, ANO6, POGLUT1, ANO10, COL22A1, MSTO1, RUNX1T1, CBLL2, AGL, MCOLN1, MSC, PPIF, MMP10, MSN, MYOD1, HLA-C, NPC1, NPPA, P2RX7, SERPINE1, PRKN, PEG3, PIK3C2A, PITX2, PLAT, HIVEP1, HCFC1, PNN, PPARD, PPID, PRG2, PKN1, MPZ, MMP9, MATR3, MMP8, IDH2, IL1B, IL2RB, IMPA1, INPP5B, ITPR1, ITPR3, KRT14, LAMB2, LCN2, LGALS3, HLA-E, LMNB1, LPA, SMAD3, MAFD2, MBL2, MCL1, MFAP1, MAP2K6, RAG1, RAG2, PLAAT4, WNT7A, CNBP, PABPN1, GCY, TNFSF11, TNFRSF11A, BANF1, DPM2, SYNJ1, SYNJ2, MGAM, FMR1, HP, KL, ADIPOQ, ESR2, GOSR2, ENO1, HDAC9, GEM, VDAC3, GH1, GJB1, REN, BRD2, ROS1, GPT, S100B, SDC2, GLB1, GJB2, SHOX, TIMP1, SI, SMN1, SNTB1, SOD1, SPN, STIM1, TERF1, TGFB1, ABCA4
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Accelerated Phase Chronic Myelogenous Leukemia
Wikipedia
External links [ edit ] Accelerated phase chronic myelogenous leukemia entry in the public domain NCI Cancer Dictionary Classification D MeSH : D015465 v t e Myeloid -related hematological malignancy CFU-GM / and other granulocytes CFU-GM Myelocyte AML : Acute myeloblastic leukemia M0 M1 M2 APL/M3 MP Chronic neutrophilic leukemia Monocyte AML AMoL/M5 Myeloid dendritic cell leukemia CML Philadelphia chromosome Accelerated phase chronic myelogenous leukemia Myelomonocyte AML M4 MD-MP Juvenile myelomonocytic leukemia Chronic myelomonocytic leukemia Other Histiocytosis CFU-Baso AML Acute basophilic CFU-Eos AML Acute eosinophilic MP Chronic eosinophilic leukemia / Hypereosinophilic syndrome MEP CFU-Meg MP Essential thrombocytosis Acute megakaryoblastic leukemia CFU-E AML Erythroleukemia/M6 MP Polycythemia vera MD Refractory anemia Refractory anemia with excess of blasts Chromosome 5q deletion syndrome Sideroblastic anemia Paroxysmal nocturnal hemoglobinuria Refractory cytopenia with multilineage dysplasia CFU-Mast Mastocytoma Mast cell leukemia Mast cell sarcoma Systemic mastocytosis Mastocytosis : Diffuse cutaneous mastocytosis Erythrodermic mastocytosis Adult type of generalized eruption of cutaneous mastocytosis Urticaria pigmentosa Mast cell sarcoma Solitary mastocytoma Systemic mastocytosis Xanthelasmoidal mastocytosis Multiple/unknown AML Acute panmyelosis with myelofibrosis Myeloid sarcoma MP Myelofibrosis Acute biphenotypic leukaemia This oncology article is a stub .
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Congenital Muscular Dystrophy, Fukuyama Type
Orphanet
Brain, cerebellar and ocular abnormalities observed in most FCMD patients are similar to and would be diagnosed out of Japan as MEB syndrome (see this term). Therefore, there is an increasing tendency to use the global term MEB/FCMD syndrome.
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Diffuse Cutaneous Systemic Sclerosis
Orphanet
Differential diagnosis Differential diagnoses include Sharp syndrome, systemic lupus erythematosus, antiphospholipid syndrome, polyarteritis nodosa, polymyositis, and rheumatoid arthritis (see these terms).HLA-DRB1, CCN2, IRF5, CCR6, CAV1, VAC14, MIF, RBM45, BANK1, TGFB1, IL13, PSS, FN1, GYPA, WDHD1, STAT4, CTLA4, TOP1, EIF2B4, EIF2B2, EIF2S2, CD163, BTG3, SS18L1, RARRES2, ICOS, CYCS, CRP, COL1A1, CRLF2, TSLP, CCR7, COL22A1, CCL4, PTEN, HEXA, IL10, HLA-DMA, HLA-DQA1, HLA-DQB1, IFI16, IFNG, IL1A, IL1B, IL6, FBN1, PRTN3, CXCL10, EIF2B1, CD180, EGFR, MPO, PECAM1, PGF, POMC, CAT
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Punding
Wikipedia
Find sources: "Punding" – news · newspapers · books · scholar · JSTOR ( December 2019 ) Punding, a possible symptom of dopamine dysregulation syndrome (DDS), is the repetition of complex motor behaviours such as collecting or arranging objects. ... "Punding in Parkinson's disease: its relation to the dopamine dysregulation syndrome". Mov. Disord . 19 (4): 397–405. doi : 10.1002/mds.20045 .
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Digestive System Neoplasm
Wikipedia
Types include: esophageal cancer gastric cancer small intestinal cancer colorectal cancer anal cancer References [ edit ] External links [ edit ] Classification D ICD - 10 : C15 - C26 D12 - D13 MeSH : D004067 v t e Overview of tumors , cancer and oncology Conditions Benign tumors Hyperplasia Cyst Pseudocyst Hamartoma Malignant progression Dysplasia Carcinoma in situ Cancer Metastasis Primary tumor Sentinel lymph node Topography Head and neck ( oral , nasopharyngeal ) Digestive system Respiratory system Bone Skin Blood Urogenital Nervous system Endocrine system Histology Carcinoma Sarcoma Blastoma Papilloma Adenoma Other Precancerous condition Paraneoplastic syndrome Staging / grading TNM Ann Arbor Prostate cancer staging Gleason grading system Dukes classification Carcinogenesis Cancer cell Carcinogen Tumor suppressor genes / oncogenes Clonally transmissible cancer Oncovirus Carcinogenic bacteria Misc. Research Index of oncology articles History Cancer pain Cancer and nausea 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 This article about a neoplasm is a stub .
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Fear Of Crossing Streets
Wikipedia
., a normal learning behavior) rather than fear (which is an abnormal avoidant behavior). [4] Fear of crossing streets may also result from an anticipatory anxiety related to person's limited mobility due to stiff person syndrome (SPS). In fact a person with SPS crossing a street may develop attacks of increasing stiffness or spasms . [5] Dromophobia may be present in people, especially children, with autism , since crossing a road involves complex skills, such as judging the speed of an approaching car. [6] See also [ edit ] Incident stress Further reading [ edit ] Szasz, Thomas. ... ISBN 1134905963 – via Google Books. ^ Rodrigues de Cerqueira, Ana Claudia; Ferreira Becerra, José Marcelo; Rozentha, Márcia; Emídio Nardi, Antônio (August 2010). "Stiff-Person Syndrome and Generalized Anxiety Disorder" .
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Hypospermia
Wikipedia
PMID 18801689 . 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 about a disease of the genitourinary system is a stub .
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Carbon Stain
Wikipedia
ISBN 978-0-7216-2921-6 . v t e Cutaneous keratosis, ulcer, atrophy, and necrobiosis Epidermal thickening keratoderma : Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis : Seborrheic keratosis Clonal seborrheic keratosis Common seborrheic keratosis Irritated seborrheic keratosis Seborrheic keratosis with squamous atypia Reticulated seborrheic keratosis Dermatosis papulosa nigra Keratosis punctata of the palmar creases other hyperkeratosis : Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar keratosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Keloid Hypertrophic scar Cutis verticis gyrata Necrobiosis / granuloma Necrobiotic/palisading Granuloma annulare Perforating Generalized Subcutaneous Granuloma annulare in HIV disease Localized granuloma annulare Patch-type granuloma annulare Necrobiosis lipoidica Annular elastolytic giant-cell granuloma Granuloma multiforme Necrobiotic xanthogranuloma Palisaded neutrophilic and granulomatous dermatitis Rheumatoid nodulosis Interstitial granulomatous dermatitis / Interstitial granulomatous drug reaction Foreign body granuloma Beryllium granuloma Mercury granuloma Silica granuloma Silicone granuloma Zirconium granuloma Soot tattoo Tattoo Carbon stain Other/ungrouped eosinophilic dermatosis Granuloma faciale Dermis / localized CTD Cutaneous lupus erythematosus chronic: Discoid Panniculitis subacute : Neonatal ungrouped: Chilblain Lupus erythematosus–lichen planus overlap syndrome Tumid Verrucous Rowell's syndrome Scleroderma / Morphea Localized scleroderma Localized morphea Morphea–lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma Atrophic / atrophoderma Lichen sclerosus Anetoderma Schweninger–Buzzi anetoderma Jadassohn–Pellizzari anetoderma Atrophoderma of Pasini and Pierini Acrodermatitis chronica atrophicans Semicircular lipoatrophy Follicular atrophoderma Linear atrophoderma of Moulin Perforating Kyrle disease Reactive perforating collagenosis Elastosis perforans serpiginosa Perforating folliculitis Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum / Pseudo-ainhum This cutaneous condition article is a stub .
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Follicular Atrophoderma
Wikipedia
External links [ edit ] Classification D ICD - 10 : L90.8 ( ILDS L90.820) v t e Cutaneous keratosis, ulcer, atrophy, and necrobiosis Epidermal thickening keratoderma : Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis : Seborrheic keratosis Clonal seborrheic keratosis Common seborrheic keratosis Irritated seborrheic keratosis Seborrheic keratosis with squamous atypia Reticulated seborrheic keratosis Dermatosis papulosa nigra Keratosis punctata of the palmar creases other hyperkeratosis : Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar keratosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Keloid Hypertrophic scar Cutis verticis gyrata Necrobiosis / granuloma Necrobiotic/palisading Granuloma annulare Perforating Generalized Subcutaneous Granuloma annulare in HIV disease Localized granuloma annulare Patch-type granuloma annulare Necrobiosis lipoidica Annular elastolytic giant-cell granuloma Granuloma multiforme Necrobiotic xanthogranuloma Palisaded neutrophilic and granulomatous dermatitis Rheumatoid nodulosis Interstitial granulomatous dermatitis / Interstitial granulomatous drug reaction Foreign body granuloma Beryllium granuloma Mercury granuloma Silica granuloma Silicone granuloma Zirconium granuloma Soot tattoo Tattoo Carbon stain Other/ungrouped eosinophilic dermatosis Granuloma faciale Dermis / localized CTD Cutaneous lupus erythematosus chronic: Discoid Panniculitis subacute : Neonatal ungrouped: Chilblain Lupus erythematosus–lichen planus overlap syndrome Tumid Verrucous Rowell's syndrome Scleroderma / Morphea Localized scleroderma Localized morphea Morphea–lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma Atrophic / atrophoderma Lichen sclerosus Anetoderma Schweninger–Buzzi anetoderma Jadassohn–Pellizzari anetoderma Atrophoderma of Pasini and Pierini Acrodermatitis chronica atrophicans Semicircular lipoatrophy Follicular atrophoderma Linear atrophoderma of Moulin Perforating Kyrle disease Reactive perforating collagenosis Elastosis perforans serpiginosa Perforating folliculitis Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum / Pseudo-ainhum This Genodermatoses article is a stub .
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Silica Granuloma
Wikipedia
External links [ edit ] Classification D ICD - 10 : L92.8 ( ILDS L92.874) v t e Cutaneous keratosis, ulcer, atrophy, and necrobiosis Epidermal thickening keratoderma : Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis : Seborrheic keratosis Clonal seborrheic keratosis Common seborrheic keratosis Irritated seborrheic keratosis Seborrheic keratosis with squamous atypia Reticulated seborrheic keratosis Dermatosis papulosa nigra Keratosis punctata of the palmar creases other hyperkeratosis : Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar keratosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Keloid Hypertrophic scar Cutis verticis gyrata Necrobiosis / granuloma Necrobiotic/palisading Granuloma annulare Perforating Generalized Subcutaneous Granuloma annulare in HIV disease Localized granuloma annulare Patch-type granuloma annulare Necrobiosis lipoidica Annular elastolytic giant-cell granuloma Granuloma multiforme Necrobiotic xanthogranuloma Palisaded neutrophilic and granulomatous dermatitis Rheumatoid nodulosis Interstitial granulomatous dermatitis / Interstitial granulomatous drug reaction Foreign body granuloma Beryllium granuloma Mercury granuloma Silica granuloma Silicone granuloma Zirconium granuloma Soot tattoo Tattoo Carbon stain Other/ungrouped eosinophilic dermatosis Granuloma faciale Dermis / localized CTD Cutaneous lupus erythematosus chronic: Discoid Panniculitis subacute : Neonatal ungrouped: Chilblain Lupus erythematosus–lichen planus overlap syndrome Tumid Verrucous Rowell's syndrome Scleroderma / Morphea Localized scleroderma Localized morphea Morphea–lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma Atrophic / atrophoderma Lichen sclerosus Anetoderma Schweninger–Buzzi anetoderma Jadassohn–Pellizzari anetoderma Atrophoderma of Pasini and Pierini Acrodermatitis chronica atrophicans Semicircular lipoatrophy Follicular atrophoderma Linear atrophoderma of Moulin Perforating Kyrle disease Reactive perforating collagenosis Elastosis perforans serpiginosa Perforating folliculitis Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum / Pseudo-ainhum This cutaneous condition article is a stub .
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Localized Granuloma Annulare
Wikipedia
ISBN 978-0-7216-2921-6 . v t e Cutaneous keratosis, ulcer, atrophy, and necrobiosis Epidermal thickening keratoderma : Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis : Seborrheic keratosis Clonal seborrheic keratosis Common seborrheic keratosis Irritated seborrheic keratosis Seborrheic keratosis with squamous atypia Reticulated seborrheic keratosis Dermatosis papulosa nigra Keratosis punctata of the palmar creases other hyperkeratosis : Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar keratosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Keloid Hypertrophic scar Cutis verticis gyrata Necrobiosis / granuloma Necrobiotic/palisading Granuloma annulare Perforating Generalized Subcutaneous Granuloma annulare in HIV disease Localized granuloma annulare Patch-type granuloma annulare Necrobiosis lipoidica Annular elastolytic giant-cell granuloma Granuloma multiforme Necrobiotic xanthogranuloma Palisaded neutrophilic and granulomatous dermatitis Rheumatoid nodulosis Interstitial granulomatous dermatitis / Interstitial granulomatous drug reaction Foreign body granuloma Beryllium granuloma Mercury granuloma Silica granuloma Silicone granuloma Zirconium granuloma Soot tattoo Tattoo Carbon stain Other/ungrouped eosinophilic dermatosis Granuloma faciale Dermis / localized CTD Cutaneous lupus erythematosus chronic: Discoid Panniculitis subacute : Neonatal ungrouped: Chilblain Lupus erythematosus–lichen planus overlap syndrome Tumid Verrucous Rowell's syndrome Scleroderma / Morphea Localized scleroderma Localized morphea Morphea–lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma Atrophic / atrophoderma Lichen sclerosus Anetoderma Schweninger–Buzzi anetoderma Jadassohn–Pellizzari anetoderma Atrophoderma of Pasini and Pierini Acrodermatitis chronica atrophicans Semicircular lipoatrophy Follicular atrophoderma Linear atrophoderma of Moulin Perforating Kyrle disease Reactive perforating collagenosis Elastosis perforans serpiginosa Perforating folliculitis Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum / Pseudo-ainhum This cutaneous condition article is a stub .