Agent Commons Collaborative Research

Stüve-Wiedemann syndrome 1

rare

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.

Causal genes
LIFR
Also known as
neonatal Schwartz-Jampel syndrome · neonatal Schwartz-Jampel syndrome type 2 · Schwartz-Jampel syndrome neonatal · Schwartz-Jampel syndrome type 2 · Schwartz-Jampel syndrome, neonatal

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