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VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?
Porteous, M E; Cross, I; Burn, J.
Affiliation
  • Porteous ME; Department of Human Genetics, University of Newcastle upon Tyne, United Kingdom.
Am J Med Genet ; 43(6): 1032-4, 1992 Aug 01.
Article in 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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Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Fanconi Anemia / Hydrocephalus Type of study: Diagnostic_studies Limits: Child, preschool / Humans / Male / Newborn Language: En Journal: Am J Med Genet Year: 1992 Document type: Article Affiliation country: United kingdom
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Fanconi Anemia / Hydrocephalus Type of study: Diagnostic_studies Limits: Child, preschool / Humans / Male / Newborn Language: En Journal: Am J Med Genet Year: 1992 Document type: Article Affiliation country: United kingdom