Síndrome de Cohen: asociación no casual con anillos vasculares

  1. C. Pérez-Caballero Macarrón
  2. C. Lozano Giménez
  3. A. Quintana Castilla
  4. J.M. Aparicio Meix
Revista:
Anales de Pediatría: Publicación Oficial de la Asociación Española de Pediatría ( AEP )

Ano de publicación: 2000

Volume: 52

Número: 3

Páxinas: 289-295

Tipo: Artigo

DOI: 10.1016/S1695-4033(00)77342-5 DIALNET GOOGLE SCHOLAR lock_openAcceso aberto editor

Resumo

Cohen syndrome is an autosomal recessive disorder characterized by hypotonia, mental retardation, microcephalia, typical craniofacial features, myopia and chorioretinal dystrophy. The responsible gene has been mapped to chromosome 8q 22 (COH 1). Since it was described more than 100 patients have been reported. However, none of them has been associated with vascular rings. Our hospital has studied eight pediatric cases and 25% of them were related wiyh vascular rings.

Fonte de datos: Dialnet