Stüve-Wiedemann syndrome 1

A rare autosomal recessive congenital primary skeletal dysplasia, characterized by small stature, bowing of the long bones, camptodactyly, hyperthermic episodes, respiratory distress/apneic episodes and feeding difficulties that usually lead to early mortality.

Also known as: STUVE-Wiedemann syndrome, SWS, Stuve-Wiedemann syndrome, Stws, Stüve-Wiedemann syndrome, SJS2, STWS, Schwartz-Jampel syndrome neonatal

35 clinical trials for this condition and its sub-types.