varadi papp syndrome, an unusual variant of oral-facial-digital syndrome: report of a rare case
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2013
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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.
| Reference Key |
patra2013annalsvaradi
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|---|---|
| Authors | ;Soumya Patra;Radheshyam Purkait;Tryambak Samanta;Ramchandra Bhadra |
| Journal | Journal of global antimicrobial resistance |
| Year | 2013 |
| DOI |
10.4103/0972-2327.112502
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