Oesophageal atresia, VACTERL association: Fanconi's anaemia related spectrum of anomalies
- PMID: 9623406
- PMCID: PMC1717521
- DOI: 10.1136/adc.78.4.375
Oesophageal atresia, VACTERL association: Fanconi's anaemia related spectrum of anomalies
Abstract
Oesophageal atresia usually occurs without any genetic background. Three cases associated with Fanconi's anaemia are reported. One neonate had growth retardation and numerous malformations including oesophageal atresia and four other components of the VACTERL association. In the two others, oesophageal atresia was isolated. In patients with such malformations an early diagnosis of Fanconi's anaemia may have important genetic and therapeutic implications.
Comment in
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Oesophageal atresia, VACTERL association: Fanconi's anaemia related spectrum of anomalies.Arch Dis Child. 1999 Feb;80(2):207. doi: 10.1136/adc.80.2.207. Arch Dis Child. 1999. PMID: 10325745 Free PMC article. No abstract available.
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