VACTERL with hydrocephalus: One end of the Fanconi anemia spectrum of anomalies?
- 1 August 1992
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 43 (6) , 1032-1034
- https://doi.org/10.1002/ajmg.1320430624
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.Keywords
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