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Harlequin ichthyosis

ORPHA:457DiseaseAutosomal recessiveNeonatal

Ассоциированные гены (1)

ABCA12
ATP binding cassette subfamily A member 12
Disease-causing germline mutation(s) in
OMIM: 607800

Фенотипы (18)

Очень частый (80–99%)7
HP:0000364Hearing abnormality
HP:0000457Depressed nasal ridge
HP:0000656Ectropion
HP:0000962Hyperkeratosis
HP:0002205Recurrent respiratory infections
HP:0007431Congenital ichthyosiform erythroderma
HP:0008064Ichthyosis
Частый (30–79%)3
HP:0001019Erythroderma
HP:0001376Limitation of joint mobility
HP:0012472Eclabion
Периодический (5–29%)8
HP:0000518Cataract
HP:0001161Hand polydactyly
HP:0001645Sudden cardiac death
HP:0001829Foot polydactyly
HP:0001944Dehydration
HP:0002047Malignant hyperthermia
HP:0002093Respiratory insufficiency
HP:0100716Self-injurious behavior

Эпидемиология (2)

Point prevalence
Unknown
Worldwide
Cases/families
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы