Two unrelated patients with autosomal dominant omodysplasia and FRIZZLED2 mutations
Hannah E Warren1, Raymond J Louie1, Michael J Friez1
1Greenwood Genetic Center Greenwood South Carolina.
Clinical Case Reports
|November 21, 2018
Abstract:
Presented are two patients with autosomal dominant omodysplasia and mutations in the FZD2 gene. The mutations identified have been recently reported, suggesting the possibility of recurrent mutations. The phenotypes of these patients overlap with what has been previously reported, though intellectual disability as seen in our patient is not typical.
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