1.
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.