Annals of Indian Academy of Neurology
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CASE REPORT
Year : 2013  |  Volume : 16  |  Issue : 2  |  Page : 289-291

Varadi Papp syndrome, an unusual variant of oral-facial-digital syndrome: Report of a rare case


1 Department of Pediatric Medicine, NRS Medical College and Hospital, Kolkata, India
2 Department of Radiology, NRS Medical College and Hospital, Kolkata, India

Correspondence Address:
Soumya Patra
RMO cum Clinical Tutor, N.R.S Medical College, 138, AJC Bose Road, Kolkata - 700014, West Bengal
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0972-2327.112502

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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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