VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?
Am J Med Genet
; 43(6): 1032-4, 1992 Aug 01.
Article
en En
| MEDLINE
| ID: mdl-1415330
ABSTRACT
Two cases of Fanconi anemia presenting as hydrocephalus are discussed. Both infants had initially been considered to have features of VACTERL. Chromosomal breakage studies should be performed in all cases of VACTERL with hydrocephalus so that Fanconi anemia may be excluded.
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Banco de datos:
MEDLINE
Asunto principal:
Anomalías Múltiples
/
Anemia de Fanconi
/
Hidrocefalia
Tipo de estudio:
Diagnostic_studies
Límite:
Child, preschool
/
Humans
/
Male
/
Newborn
Idioma:
En
Revista:
Am J Med Genet
Año:
1992
Tipo del documento:
Article
País de afiliación:
Reino Unido