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ORPHA:1122· ICD-10 Q73.8· Ulnar hypoplasia-split foot syndrome

Визначення(English summary)

Ulnar hypoplasia-split foot syndrome is characterised by the association of severe ulnar hypoplasia, absence of fingers two to five, and split-foot. It has been described in four males belonging to two generations of the same family. X-linked recessive inheritance is suggested, but autosomal dominant transmission cannot be excluded.

Поширеність
<1 / 1 000 000
Вік початку
Neonatal