Oesophageal atresia in the South West of England

T. J. David, S. E. O'Callaghan

    Research output: Contribution to journalArticlepeer-review

    Abstract

    A retrospective anatomical and family study was made of 345 patients with oesophageal atresia who were born in the South West of England between 1942 and 1973. There were 186 males and 159 females. Twenty one cases were stillborn. Eighty five % of the patients had a combination of oesophageal atresia with a tracheo oesophageal fistula to the distal oesophageal segment, and 9% had atresia without a fistula. Fifty five % of the patients had other congenital malformations and these tended to be multiple rather than single. Thirty six % of singletons had unequivocal fetal growth retardation, and there is some evidence that nearly all cases have poor fetal growth. There appeared to be a maternal age effect, with an excess of mothers under 20 and over 35, and there was an unexplained excess of fathers employed in the Armed Forces. Ten % of the cases were illegitimate. There were 21 twins which is nearly 3 times the expected number; there were 2 pairs of twins concordant for oesophageal atresia, one being monozygotic and the other dizygotic. In one case there were 2 sibs with oesophageal atresia. Five out of 365 sibs had anencephaly. The blood group distributions of the patients and their mothers did not significantly differ from the expected distribution. Oesophageal atresia is aetiologically heterogenous. In this series there were at least 5, and probably 10 cases of trisomy 18, and 4 cases of trisomy 21. Five mothers had overt diabetes, and there is some suggestion from other work that maternal diabetes or its treatment may be aetiologically important. Oesophageal atresia was part of a possibly recessively inherited malformation syndrome in 2 cases. A sibship with a case of rectal atresia, a case of Hirschprung's disease and a case of oesophageal atresia may represent the action of another recessive gene. It seems likely that oesophageal atresia is a rather nonspecific consequence of several teratological processes.
    Original languageEnglish
    Pages (from-to)1-11
    Number of pages10
    JournalJournal of Medical Genetics
    Volume12
    Issue number1
    Publication statusPublished - 1975

    Fingerprint

    Dive into the research topics of 'Oesophageal atresia in the South West of England'. Together they form a unique fingerprint.

    Cite this