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Спектр дефіциту GATA2

ORPHA:228423· ICD-10 D72.8· GATA2 deficiency spectrum

Визначення(English summary)

A rare genetic primary immunodeficiency characterized by profound circulating monocytopenia, B- and NK-cell lymphopenia and severe dentritic cell decrease, which manifests clinically with disseminated mycobacterial and viral infections, as well as opportunistic fungal and parasitic infections and frequent pulmonary alveolar proteinosis. Predisposition to developping myeloid neoplasms is associated.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal dominant, Not applicable
Вік початку
Adult