Microvillous inclusion disease: How to improve the prognosis of a severe congenital enterocyte disorder

Journal of Pediatric Gastroenterology and Nutrition

Volumn 52, Issue 4, 2011, Pages 460-465

  Halac, Ugur ^a   Lacaille, Florence ^a   Joly, Francisca ^b   Hugot, Jean Pierre ^c   Talbotec, Cécile ^a   Colomb, Virginie ^a   Ruemmele, Frank M ^a   Goulet, Olivier ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b BEAUJON HOSPITAL   (France)

^c HÔPITAL ROBERT DEBRÉ   (France)

Author keywords

congenital diarrhea; microvillous inclusion disease; small bowel transplantation

Indexed keywords

ARTICLE; CHILD; CLINICAL ARTICLE; CONGENITAL DISORDER; CONSANGUINEOUS MARRIAGE; DEVELOPMENTAL DISORDER; ENTEROCYTE DISORDER; FEMALE; GROWTH DISORDER; HUMAN; INTESTINE TRANSPLANTATION; KIDNEY DISEASE; LIVER FIBROSIS; MALE; MICROVILLOUS INCLUSION DISEASE; MICROVILLUS; MORTALITY; PARENTERAL NUTRITION; PRIORITY JOURNAL; PROGNOSIS;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; FEMALE; HOSPITALS, PEDIATRIC; HUMANS; INCLUSION BODIES; INFANT; INFANT, NEWBORN; INTESTINE, SMALL; MALABSORPTION SYNDROMES; MALE; MEDITERRANEAN REGION; MICROVILLI; MUCOLIPIDOSES; PARENTERAL NUTRITION; PROGNOSIS; RETROSPECTIVE STUDIES; SURVIVAL ANALYSIS; TREATMENT OUTCOME;

EID: 79953830081     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/MPG.0b013e3181fb4559     Document Type: Article

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