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
Zeitschrift:
Anales de Pediatría: Publicación Oficial de la Asociación Española de Pediatría ( AEP )

Datum der Publikation: 2000

Ausgabe: 52

Nummer: 3

Seiten: 289-295

Art: Artikel

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

Zusammenfassung

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.

Fuente de los datos: Dialnet