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Indian Pediatr ; 2011 September; 48(9): 731-732
Artículo en Inglés | IMSEAR | ID: sea-168962

RESUMEN

Wiedemann-Rautenstauch (WR) syndrome is a rare autosomal recessive neonatal progeroid syndrome with only few published case reports. We describe a neonate showing clinical features of WR syndrome with peeling of skin, and presented with weak cry and breathing difficulty since birth.

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