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Pubmed for Handhelds

PUBMED FOR HANDHELDS

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  • Title: Type III syndactyly and oculodentodigital dysplasia: a clinical spectrum.
    Author: Schrander-Stumpel CT, De Groot-Wijnands JB, De Die-Smulders C, Fryns JP.
    Journal: Genet Couns; 1993; 4(4):271-6. PubMed ID: 8110413.
    Abstract:
    A newborn male patient presented with complete cutaneous syndactyly of fingers 3-5 in the left hand and fingers 4-5 in the right hand. The mother and maternal grandmother were born with the same hand malformation. Facial features in the mother showed a thin nose and small teeth; eyes were normal. In the grandmother, teeth had been very small with enamel hypoplasia; eyes were normal. The present family provides evidence of the variable expression in oculodentodigital dysplasia. Inheritance is autosomal dominant.
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