Achondrogenesis type 2

Orpha code: 93296OMIM code: 200610

Definicja

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.

Disease data
Klasyfikacja

Clinical subtype

Synonimy
Achondrogenesis, Langer-Saldino type
Achondrogeneza typu Langera i Saldino
Kod ORPHA
93296
Kod OMIM
200610
Kod ICD10
Q77.0
Kod ICD11
-

No additional description.

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