| CASE REPORT |
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| Year : 2013 | Volume
: 16
| Issue : 2 | Page : 289-291 |
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Varadi Papp syndrome, an unusual variant of oral-facial-digital syndrome: Report of a rare case
Soumya Patra1, Radheshyam Purkait1, Tryambak Samanta1, Ramchandra Bhadra2
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
 Source of Support: None, Conflict of Interest: None  | Check |
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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