Hirschsprung’s disease in children with Mowat–Wilson syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Surgery,Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00383-015-3732-x.pdf
Reference60 articles.
1. Holschneider AM, Puri P (2008) Hirschsprung’s disease and allied disorders, 3rd edn. Springer, Berlin, Heidelberg
2. Mowat DR, Croaker GD, Cass DT, Kerr BA, Chaitow J, Ades LC, Chia NL, Wilson MJ (1998) Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23. J Med Genet 35(8):617–623
3. Yamada Y, Nomura N, Yamada K, Matsuo M, Suzuki Y, Sameshima K, Kimura R, Yamamoto Y, Fukushi D, Fukuhara Y, Ishihara N, Nishi E, Imataka G, Suzumura H, Hamano S, Shimizu K, Iwakoshi M, Ohama K, Ohta A, Wakamoto H, Kajita M, Miura K, Yokochi K, Kosaki K, Kuroda T, Kosaki R, Hiraki Y, Saito K, Mizuno S, Kurosawa K, Okamoto N, Wakamatsu N (2014) The spectrum of ZEB2 mutations causing the Mowat–Wilson syndrome in Japanese populations. Am J Med Genet A 164A(8):1899–1908. doi: 10.1002/ajmg.a.36551
4. Kenny SE, Tam PK, Garcia-Barcelo M (2010) Hirschsprung’s disease. Semin Pediatr Surg 19(3):194–200. doi: 10.1053/j.sempedsurg.2010.03.004
5. Friedmacher F, Puri P (2013) Hirschsprung’s disease associated with Down syndrome: a meta-analysis of incidence, functional outcomes and mortality. Pediatr Surg Int 29(9):937–946. doi: 10.1007/s00383-013-3361-1
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