Outcomes of Hirschsprung's disease associated with Mowat-Wilson syndrome

Journal of Pediatric Surgery

Volumn 44, Issue 3, 2009, Pages 587-591

  Bonnard, Arnaud ^a   Zeidan, Smart ^a   Degas, Vanessa ^a   Viala, Jérome ^a   Baumann, Clarisse ^a   Berrebi, Dominique ^a   Perrusson, Odile ^a   El Ghoneimi, Alaa ^a  

^a HÔPITAL ROBERT DEBRÉ   (France)

Author keywords

Hirschsprung's disease; Motility disorder; Mowat Wilson syndrome

Indexed keywords

2Q22 GENE; ADULT; AGANGLIONOSIS; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DISEASE SEVERITY; DUHAMEL PROCEDURE; ENTEROCOLITIS; FEMALE; FOLLOW UP; GENE; GENE DELETION; GENETIC DISORDER; HIRSCHSPRUNG DISEASE; HUMAN; INTESTINE MOTILITY; MALE; MENTAL DEFICIENCY; MOTOR DEVELOPMENT; NONSENSE MUTATION; OUTCOME ASSESSMENT; PRIORITY JOURNAL; PULL THROUGH OPERATION; RETROSPECTIVE STUDY; SIGMOIDOSCOPY; SIP1 GENE; SURGICAL TECHNIQUE; TOTAL PARENTERAL NUTRITION; WILSON DISEASE;

DEVELOPMENTAL DISABILITIES; FEMALE; HEAD; HIRSCHSPRUNG DISEASE; HUMANS; INFANT, NEWBORN; MALE; MENTAL RETARDATION; PARENTERAL NUTRITION, TOTAL; RETROSPECTIVE STUDIES; SYNDROME;

EID: 62549143101     PISSN: 00223468     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpedsurg.2008.10.066     Document Type: Article

References (10)

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