Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Adicionar filtros








Intervalo de ano
1.
Indian Pediatr ; 2011 September; 48(9): 731-732
Artigo em Inglês | IMSEAR | ID: sea-168962

RESUMO

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.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA