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  • Title: Varadi Papp syndrome, an unusual variant of oral-facial-digital syndrome: Report of a rare case.
    Author: Patra S, Purkait R, Samanta T, Bhadra R.
    Journal: Ann Indian Acad Neurol; 2013 Apr; 16(2):289-91. PubMed ID: 23956587.
    Abstract:
    Varadi Papp syndrome or oral-facial-digital syndrome type VI (OFDS VI) is a rare autosomal-recessive disorder distinguished from other OFDSs by metacarpal abnormalities with central polydactyly and by cerebellar abnormalities. Our patient had a broad forehead, arched eyebrows, left-sided squint, hypertelorism, epicanthic folds, fleshy nodular tongue, midline upper lip cleft, high arched palate, both pre-axial and post-axial polydactyly of limbs, hypotonia and cerebellar hypoplasia with molar tooth sign consistent with the diagnosis of Varadi Papp syndrome.
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