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Синдром Чедіака-Хігаші

ORPHA:167· ICD-10 E70.3· Chédiak-Higashi syndrome

Визначення(English summary)

Chédiak-Higashi syndrome (CHS) is a rare severe genetic disorder generally characterized by partial oculocutaneous albinism (OCA, see this term), severe immunodeficiency, mild bleeding, neurological dysfunction and lymphoproliferative disorder. A classic, early-onset form and an attenuated, later-onset form (Atypical CHS; see this term) have been described.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal recessive
Вік початку
Childhood