Am J Med Genet. 1992 Aug 1;43(6):1032-4.

VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?

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Department of Human Genetics, University of Newcastle upon Tyne, United Kingdom.

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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Cited by 5 PubMed Central articles

Review VACTERL/VATER Association. [Orphanet J Rare Dis. 2011]
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VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?
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