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Longer titles found: Poikiloderma of Civatte (view), Poikiloderma vasculare atrophicans (view), Hereditary sclerosing poikiloderma (view), Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (view)

searching for Poikiloderma 9 found (38 total)

alternate case: poikiloderma

Kindler syndrome (436 words) [view diff] exact match in snippet view article find links to article

Kindler syndrome (also known as "bullous acrokeratotic poikiloderma of Kindler and Weary") is a rare congenital disease of the skin caused by a mutation

Naegeli–Franceschetti–Jadassohn syndrome (447 words) [view diff] no match in snippet view article find links to article

Naegeli–Franceschetti–Jadassohn syndrome (NFJS), also known as chromatophore nevus of Naegeli and Naegeli syndrome, is a rare autosomal dominant form of

Hereditary spastic paraplegia (3,347 words) [view diff] no match in snippet view article find links to article

Hereditary spastic paraplegia (HSP) is a group of inherited diseases whose main feature is a progressive gait disorder. The disease presents with progressive

List of diseases (P) (1,908 words) [view diff] exact match in snippet view article

retardation Poikiloderma congenital with bullae Weary type Poikiloderma hereditary acrokeratotic Weary type Poikiloderma of Kindler Poikiloderma of Rothmund–Thomson

List of diseases (N) (654 words) [view diff] exact match in snippet view article

pseudoobstruction patent ductus Nathalie syndrome Native American myopathy Navajo poikiloderma Naxos disease Necrotizing encephalopathy, infantile subacute Necrotizing

RECQL4 (1,245 words) [view diff] exact match in snippet view article find links to article

Gannavarapu A, Clericuzio CL, et al. (2004). "Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patients". Am. J. Med. Genet

List of diseases (S) (1,934 words) [view diff] exact match in snippet view article

Spastic paraplegia nephritis deafness Spastic paraplegia neuropathy poikiloderma Spastic paraplegia type 1, X-linked Spastic paraplegia type 2, X-linked

Gluten-sensitive enteropathy–associated conditions (7,556 words) [view diff] exact match in snippet view article find links to article

coeliac disease. Rothmund–Thomson syndrome. Rothmund–Thomson syndrome, or poikiloderma congenitale, is a rare disorder, generally attributed to mutations of

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

blastoma; 601200; DICER1 Pneumothorax, primary spontaneous; 173600; FLCN Poikiloderma with neutropenia; 604173; C16orf57 Polycystic kidney and hepatic disease;