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Hirschsprung’s Disease with Congenital Hypothyroidism.
Indian Pediatr ; 2012 March; 49(3): 245-246
Article Dans Anglais | IMSEAR | ID: sea-169264
ABSTRACT
We report a female newborn baby who presented with vomiting and abdominal distension on day 21 of life. Examination revealed facial puffiness, open posterior fontanelles, dry skin, cold peripheries and prominent abdominal veins with visible peristalsis. Barium enema revealed dilated proximal colon, empty rectum, funnel like transition zone between proximal dilated and distal constricted bowel. Serum TSH level was >150 μIU/mL. Biopsy revealed aganglionic segment suggesting Hirschsprung’s disease, an unusual association with congenital hypothyroidism.

Texte intégral: Disponible Indice: IMSEAR (Asie du Sud-Est) langue: Anglais Texte intégral: Indian Pediatr Année: 2012 Type: Article

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Texte intégral: Disponible Indice: IMSEAR (Asie du Sud-Est) langue: Anglais Texte intégral: Indian Pediatr Année: 2012 Type: Article