Axonal dystrophy presenting as the megacystis-microcolon-intestinal hypoperistalsis syndrome.
Pediatr Pathol
; 12(5): 743-50, 1992.
Article
en En
| MEDLINE
| ID: mdl-1437888
ABSTRACT
Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a neonatal intestinal syndrome, characterized by defective peristalsis and bladder dilatation, refractory to pharmacological treatment. Examinations of bowel and bladder have failed to demonstrate a pathological explanation for this syndrome. We describe a 7-month-old female infant with MMIHS who had generalized axonal dystrophy of her central, peripheral, and autonomic nervous systems, which may provide a neuropathological explanation for some cases of MMIHS.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Axones
/
Vejiga Urinaria
/
Colon
/
Enfermedades Intestinales
Límite:
Female
/
Humans
/
Infant
Idioma:
En
Revista:
Pediatr Pathol
Año:
1992
Tipo del documento:
Article