Browse

Explore conditions, clinical trials, and the organisations running them.

← All categories

Up to: Hereditary disease · Syndromic disease · Dysostosis · Congenital limb malformation

Ulnar hypoplasia-split foot syndrome

Ulnar hypoplasia-split foot syndrome is characterized 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.

0 trials tagged with this condition →

This condition has no sub-types.