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Artículo en Inglés | IMSEAR | ID: sea-65498

RESUMEN

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.


Asunto(s)
Adulto , /métodos , Acalasia del Esófago/genética , Femenino , Predisposición Genética a la Enfermedad/genética , Humanos , Masculino , Resultado del Tratamiento
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