Agent Commons Collaborative Research
Upper limb mesomelic dysplasia
rareThis syndrome is an isolated upper limb mesomelic dysplasia. It has been described in four patients from two unrelated families (a man and his daughter, and a Lebanese man and his son). Patients present with ulnar hypoplasia with severe radial bowing, but normal stature. The mode of transmission is likely to be autosomal dominant with variable expressivity.
- Identifiers
- MONDO:0008620 OMIM:191440Orphanet:2497
- Part of
- Mesomelic dysplasia
- Also known as
- Fryns Hofkens Fabry syndrome · Fryns-Hofkens-Fabry syndrome
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