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Коксоаурикулярний синдром

ORPHA:1508· ICD-10 Q87.1· Coxoauricular syndrome

Визначення(English summary)

A rare primary bone defect, described only in a mother and her three daughters to date, characterized by short stature, hip dislocation, minor vertebral and pelvic changes, and microtia with hearing loss. There have been no further descriptions in the literature since 1981.

Поширеність
<1 / 1 000 000
Успадкування
Unknown
Вік початку
Neonatal