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Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (Berdon Syndrome)

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An Illustrated Guide to Pediatric Urology
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Abstract

Berdon syndrome, also called Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIH syndrome), is an autosomal recessive fatal genetic disorder affecting newborns.

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Further Reading

  1. Gosemann JH, Puri P. Megacystis microcolon intestinal hypoperistalsis syndrome: systematic review of outcome. Pediatr Surg Int. 2011;27(10):1041–6.

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  2. Loinaz C, Rodríguez MM, Kato T, et al. Intestinal and multivisceral transplantation in children with severe gastrointestinal dysmotility. J Pediatr Surg. 2005;40(10):1598–604.

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  3. Mantan M, Singhal KK, Sethi GR, Aggarwal SK. Megacystis, microcolon, intestinal hypoperistalsis syndrome and bilateral streak gonads. Indian J Nephrol. 2011;21(3):212–4.

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  4. Masetti M, Rodríguez MM, Thompson JF, et al. Multivisceral transplantation for megacystis microcolon intestinal hypoperistalsis syndrome. Transplantation. 1999;68(2):228–32.

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  5. Puri P, Shinkai M. Megacystis microcolon intestinal hypoperistalsis syndrome. Semin Pediatr Surg. 2005;14(1):58–63.

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  6. Steiner SJ, Steven J. Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS). J Pediatr Gastroenterol Nutr. 2004;39(3):301.

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Al-Salem, A.H. (2017). Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (Berdon Syndrome). In: An Illustrated Guide to Pediatric Urology. Springer, Cham. https://doi.org/10.1007/978-3-319-44182-5_14

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  • DOI: https://doi.org/10.1007/978-3-319-44182-5_14

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-44181-8

  • Online ISBN: 978-3-319-44182-5

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