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Stüve-Wiedemann syndrome 1
rareA 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.
- Identifiers
- MONDO:0800043 OMIM:601559Orphanet:3206
- 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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