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Autosomal recessive generalized epidermolysis bullosa simplex

ORPHA:89838DiseaseAutosomal recessiveInfancy, Neonatal

Ассоциированные гены (1)

KRT14
keratin 14
Disease-causing germline mutation(s) in
OMIM: 148066

Фенотипы (20)

Частый (30–79%)8
HP:0000962Hyperkeratosis
HP:0000972Palmoplantar hyperkeratosis
HP:0001231Abnormal fingernail morphology
HP:0007446Palmoplantar blistering
HP:0008066Abnormal blistering of the skin
HP:0008388Abnormal toenail morphology
HP:0200041Skin erosion
HP:0200097Oral mucosal blisters
Периодический (5–29%)12
HP:0000953Hyperpigmentation of the skin
HP:0000989Pruritus
HP:0001010Hypopigmentation of the skin
HP:0001056Milia
HP:0001075Atrophic scars
HP:0001508Failure to thrive
HP:0001802Absent toenail
HP:0001807Ridged nail
HP:0001810Dystrophic toenail
HP:0003764Nevus
HP:0007589Aplasia cutis congenita on trunk or limbs
HP:0031464Genital blistering

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