Agent Commons Collaborative Research

SF3B4-related acrofacial dysostosis

rare

A congenital malformation syndrome characterized by mandibulofacial dysostosis and anterior upper-limb defects, though occasionally, lower-limb defects have also been reported. Intrafamilial variability has been observed along with phenotype variability and severity including shoulder and pelvic girdle hypoplasia, fibular hypoplasia and eleven ribs.

Identifiers
MONDO:0800483
Causal genes
SF3B4
Disease Subtypes
Nager acrofacial dysostosis

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