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Pili torti-onychodysplasia syndrome

ORPHA:2890Malformation syndromeAutosomal recessiveInfancy, Neonatal

Фенотипы (20)

Облигатный (100%)1
HP:0000968Ectodermal dysplasia
Частый (30–79%)18
HP:0000175Cleft palate
HP:0000377Abnormal pinna morphology
HP:0000561Absent eyelashes
HP:0000958Dry skin
HP:0000964Eczematoid dermatitis
HP:0000982Palmoplantar keratoderma
HP:0001596Alopecia
HP:0002223Absent eyebrow
HP:0002289Alopecia universalis
HP:0002299Brittle hair
HP:0002552Trichodysplasia
HP:0007439Generalized keratosis follicularis
HP:0008394Congenital onychodystrophy
HP:0008404Nail dystrophy
HP:0010562Keloids
HP:0012725Cutaneous syndactyly
HP:0030953Conjunctival hyperemia
HP:0410030Cleft lip
Периодический (5–29%)1
HP:0002231Sparse body hair

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