Clinical response to the long acting somatostatin analogue SMS 201-995 in a child with congenital microvillus atrophy.

Author:

Couper R T,Berzen A,Berall G,Sherman P M

Publisher

BMJ

Subject

Gastroenterology

Reference18 articles.

1. Familial enteropathy: a syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy;I Davidson GP. Cutz E, Hamilton JR, Gall DG;Gastroenterology,1978

2. Congenital microvillus atrophy: specific diagnostic features;Phillips, A.D.; Jenkins, P.; Raafat, F.; Walker-Smith, J.A.;Arcli Dis Child,1985

3. Congenital microvillus atrophy, a rare cause of neonatal intractable diarrhoea;Schmitz, J.; Ginies, J.L.; Arnaud-Battandier, F.;[Abstracti. Pediatr Res,1982

4. Congenital and familial protracted diarrhoea with enterocyte brush border abnormalities;Goutet, J.M.; Boccon-Gibod, L.; Chatelet, F.;Pediatr Res,1982

5. Urogastrone/ epidermal growth factor in treatment of congenital microvillus atrophy;Drumm, B.; Cutz, E.; Tomkins, B.K.;Lancet,1988

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