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Artigo em Inglês | IMSEAR | ID: sea-65498

RESUMO

Familial occurrence of achalasia cardia is rare. Most associations are among siblings or in monozygotic twins. Parent-child association is even rarer and only six such instances have been reported till date. We report a 29-year-old man with achalasia cardia and his mother who had the same illness two and half years later. Both of them were successfully treated with balloon dilatation.


Assuntos
Adulto , /métodos , Acalasia Esofágica/genética , Feminino , Predisposição Genética para Doença/genética , Humanos , Masculino , Resultado do Tratamento
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