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Stiff skin syndrome

ORPHA:2833ЗаболеваниеАутосомно-доминантныйНеонатальный

Ассоциированные гены (1)

FBN1
fibrillin 1
Disease-causing germline mutation(s) in
OMIM: 134797

Фенотипы (24)

Очень частый (80–99%) — 3
HP:0001072Thickened skin
HP:0001376Limitation of joint mobility
HP:0100679Lack of skin elasticity
Частый (30–79%) — 2
HP:0000953Hyperpigmentation of the skin
HP:0000998Hypertrichosis
Периодический (5–29%) — 18
HP:0000407Sensorineural hearing impairment
HP:0000486Strabismus
HP:0000501Glaucoma
HP:0000541Retinal detachment
HP:0000787Nephrolithiasis
HP:0000822Hypertension
HP:0001324Muscle weakness
HP:0001482Subcutaneous nodule
HP:0003011Abnormality of the musculature
HP:0003119Abnormal circulating lipid concentration
HP:0004322Short stature
HP:0004325Decreased body weight
HP:0005978Type II diabetes mellitus
HP:0007328Impaired pain sensation
HP:0008065Aplasia/Hypoplasia of the skin
HP:0009830Peripheral neuropathy
HP:0011800Midface retrusion
HP:0100578Lipoatrophy
Очень редкий (1–4%) — 1
HP:0030057Autoimmune antibody positivity

Эпидемиология (2)

Cases/families
—
Worldwide
Point prevalence
<1 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы