Index finger abnormalities in Simpson-Golabi-Behmel syndrome
- PMID: 15602092
Index finger abnormalities in Simpson-Golabi-Behmel syndrome
Abstract
Simpson-Golabi-Behmel syndrome (SGBS) is an X linked recessive overgrowth disorder in which digital abnormalities are a well-described aspect of the phenotype. We report a case with marked index finger hypoplasia and a congenital abnormality of the proximal phalanx and review the literature detailing index finger abnormalities in this condition.
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