Hirschsprung's disease associated with Mowat-Wilson syndrome

BMJ Case Reports

Volumn , Issue , 2014, Pages

  Patel, Ramnik V ^a,b   Elmalik, Khalid ^c   Bouhadiba, Nordine ^c   Shawis, Rang ^c  

^a UNIVERSITY COLLEGE LONDON HOSPITALS   (United Kingdom)

^b Department of Paediatric Urology Great Ormond Street Children Hospital NHS Trust ^*  (United Kingdom)

^c Department of Paediatric Surgery Sheffiled Children's Hospital   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; COLON DILATATION; CORPUS CALLOSUM; DISEASE ASSOCIATION; EEG ABNORMALITY; FACIES; FOLLOW UP; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; HIRSCHSPRUNG DISEASE; HUMAN; HUMAN TISSUE; HYPOSPADIAS; INFANT; MALE; MECONIUM; MENTAL DEFICIENCY; MICROCEPHALY; MOWAT WILSON SYNDROME; POSTOPERATIVE PERIOD; PRIORITY JOURNAL; RECTUM BIOPSY; VOMITING; WILSON DISEASE;

EID: 84900794352     PISSN: None     EISSN: 1757790X     Source Type: Journal    
DOI: 10.1136/bcr-2013-203262     Document Type: Article

References (3)

1. Leong M, Verey F, Newbury-Ecob R, et al. Supernumerary intestinal muscle coat in a patient with Hirschsprung' s disease/Mowat-Wilson syndrome. Pediatr Dev Pathol 2010;13:415-18.
2. Cuturilo G, Stefanoviæ I, Jovanoviæ I, et al. Mowat-Wilson syndrome - a case report. Srp Arh Celok Lek 2009;137:426-9.
3. Bonnard A, Zeidan S, Degas V, et al. Outcomes of Hirschsprung 's disease associated with Mowat-Wilson syndrome. J Pediatr Surg 2009;44:587-91.