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Ахондрогенез, тип 2

ORPHA:93296· ICD-10 Q77.0· Achondrogenesis type 2

Визначення(English summary)

A rare, lethal type of achondrogenesis, and part of the spectrum of type 2 collagen-related bone disorders, characterized by severe micromelia, short neck with large head, small thorax, protuberant abdomen, underdeveloped lungs, distinctive facial features such as a prominent forehead, a small chin, a cleft palate (in some) and distinctive histological features of the cartilage.

Поширеність
Unknown
Успадкування
Autosomal dominant
Вік початку
Antenatal, Neonatal