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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 10 found (39 total)

alternate case: poikiloderma

Kindler syndrome (521 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 type of epidermolysis bullosa, a rare congenital disease

Naegeli–Franceschetti–Jadassohn syndrome (445 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

Potassium titanyl phosphate (2,087 words) [view diff] exact match in snippet view article find links to article

medical lasers for procedures like prostate surgery, dermatology (rosacea, poikiloderma, pigmentation removal, skin rejuvenation), and industrial applications

List of diseases (S) (1,933 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 (7,562 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;