Heterozygous FGFR3 c.138G>A Mutation Presenting With Achondroplasia and Hemifacial Microsomia
Hyok Jun Kwon1, Lachlan D M Farmer, Mark H Moore
1Cleft and Craniofacial South Australia, Women's and Children's Hospital, Adelaide, South Australia, Australia.
The Journal of Craniofacial Surgery
|February 16, 2024
Abstract:
We present a case of a patient with achondroplasia, hemifacial microsomia and an fibroblast growth factor receptor3 c.138G>A mutation. An association between the 2 conditions has not been previously described, but there is biological plausibility that the etiology of the 2 conditions is linked.
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