• freeman-sheldon syndrome: report of 6 cases

    جزئیات بیشتر مقاله
    • تاریخ ارائه: 1392/07/24
    • تاریخ انتشار در تی پی بین: 1392/07/24
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     freeman-sheldon syndrome is a morphologically well-defined syndrome that results in a dysmorphic status combining bone anomalies and joint contractures with characteristic facies. fss (freeman- sheldon syndrome) is also known as craniocarpotarsal dysplasia (or dystrophy), distal arthrogryposis type iia (daiia), whistling face syndrome, and whistling face-windmill vane hand syndrome. the syndrome is an autosomal dominant trait and characterized by flattened, mask-like facies, microstomia, protruding lips (as in whistling), deep-set eyes with hypertelorism, and camptodactyly with ulnar deviation of the fingers and talipes equinovarus. we are reporting 6 cases with this syndrome that were referred to our genetic center from 2000 to 2006 for cytogenetic study and clinical genetic counseling.

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