Literature DB >> 33264186

Megacystis Microcolon Intestinal Hypoperistalsis Syndrome: A Case Series With Long-term Follow-up and Prolonged Survival.

Krishnapriya Marangattu Prathapan1, Dale E King1, Vikram Kalathur Raghu1, Kimberly Ackerman1, Tracey Presel1, Jane Anne Yaworski1, Armando Ganoza2, Geoffrey Bond2, Wednesday Marie A Sevilla1, Jeffrey A Rudolph1, Feras Alissa1.   

Abstract

OBJECTIVES: Describe clinical characteristics, management, and outcome in a cohort of megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) patients.
METHODS: We conducted a retrospective chart review of MMIHS patients followed at a large transplant and intestinal rehabilitation center over a period of 17 years.
RESULTS: We identified 25 patients with MMIHS (68% girls, 13 transplanted). One transplanted and 1 nontransplanted patient were lost to follow-up. We estimated 100, 100, and 86% for 5-, 10-, and 20-year survival, respectively, with only 1 death. Of the 22 patients alive at the time of study (11 transplanted, 11 nontransplanted), median age was 9.2 years (range 2.7-22.9 years). Longest posttransplant follow-up was 16 years. Seventeen patients had available prenatal imaging reports; all showed distended bladder. Eight had genetic testing (5, ACTG2; 2, MYH11; 1, MYL9). Almost all patients had normal growth with median weight z-score -0.77 (interquartile range -1.39 to 0.26), height z score -1.2 (-2.04 to -0.48) and body mass index z-score 0.23 (-0.37 to 0.93) with no statistical difference between transplanted and nontransplanted patients. All nontransplanted patients were on parenteral nutrition with minimal/no feeds, and all except 1 of the transplanted patients were on full enteral feeds. Recent average bilirubin, INR, albumin, and creatinine fell within the reference ranges.
CONCLUSIONS: This is the largest single-center case series with the longest duration of follow-up for MMIHS patients. In the current era of improved intestinal rehabilitation and transplantation, MMIHS patients have excellent outcomes in survival, growth, and liver function. This observation contradicts previous reports and should alter counselling and management decisions in these patients at diagnosis.
Copyright © 2020 by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition.

Entities:  

Mesh:

Year:  2021        PMID: 33264186      PMCID: PMC9124153          DOI: 10.1097/MPG.0000000000003008

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   3.288


  16 in total

1.  De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis.

Authors:  Willa Thorson; Oscar Diaz-Horta; Joseph Foster; Michail Spiliopoulos; Rubén Quintero; Amjad Farooq; Susan Blanton; Mustafa Tekin
Journal:  Hum Genet       Date:  2013-12-13       Impact factor: 4.132

2.  Newly described recessive MYH11 disorder with clinical overlap of Multisystemic smooth muscle dysfunction and Megacystis microcolon hypoperistalsis syndromes.

Authors:  Anji T Yetman; Lois J Starr
Journal:  Am J Med Genet A       Date:  2018-04       Impact factor: 2.802

3.  Megacystis-microcolon-intestinal hypoperistalsis syndrome: a new cause of intestinal obstruction in the newborn. Report of radiologic findings in five newborn girls.

Authors:  W E Berdon; D H Baker; W A Blanc; B Gay; T V Santulli; C Donovan
Journal:  AJR Am J Roentgenol       Date:  1976-05       Impact factor: 3.959

Review 4.  Megacystis-microcolon-intestinal hypoperistalsis syndrome: case report and review of prenatal ultrasonographic findings.

Authors:  Lea Tuzovic; Kwame Anyane-Yeboa; Ashley Mills; Kenneth Glassberg; Russell Miller
Journal:  Fetal Diagn Ther       Date:  2014-02-21       Impact factor: 2.587

5.  Homozygous deletion in MYL9 expands the molecular basis of megacystis-microcolon-intestinal hypoperistalsis syndrome.

Authors:  Carolina Araujo Moreno; Nara Sobreira; Elizabeth Pugh; Peng Zhang; Gary Steel; Fábio Rossi Torres; Denise Pontes Cavalcanti
Journal:  Eur J Hum Genet       Date:  2018-02-16       Impact factor: 4.246

Review 6.  Megacystis microcolon intestinal hypoperistalsis syndrome: Case series and updated review of the literature with an emphasis on urologic management.

Authors:  Kevin M Wymer; Blake B Anderson; Ashley A Wilkens; Mohan S Gundeti
Journal:  J Pediatr Surg       Date:  2016-06-26       Impact factor: 2.545

7.  A homozygous loss-of-function variant in MYH11 in a case with megacystis-microcolon-intestinal hypoperistalsis syndrome.

Authors:  Julie Gauthier; Bouchra Ouled Amar Bencheikh; Fadi F Hamdan; Steven M Harrison; Linda A Baker; Françoise Couture; Isabelle Thiffault; Reda Ouazzani; Mark E Samuels; Grant A Mitchell; Guy A Rouleau; Jacques L Michaud; Jean-François Soucy
Journal:  Eur J Hum Genet       Date:  2014-11-19       Impact factor: 4.246

8.  Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndrome.

Authors:  Michael F Wangler; Claudia Gonzaga-Jauregui; Tomasz Gambin; Samantha Penney; Timothy Moss; Atul Chopra; Frank J Probst; Fan Xia; Yaping Yang; Steven Werlin; Ieva Eglite; Liene Kornejeva; Carlos A Bacino; Dustin Baldridge; Jeff Neul; Efrat Lev Lehman; Austin Larson; Joke Beuten; Donna M Muzny; Shalini Jhangiani; Richard A Gibbs; James R Lupski; Arthur Beaudet
Journal:  PLoS Genet       Date:  2014-03-27       Impact factor: 5.917

9.  Compound heterozygous variants in MYH11 underlie autosomal recessive megacystis-microcolon-intestinal hypoperistalsis syndrome in a Chinese family.

Authors:  Qin Wang; Jianming Zhang; Hui Wang; Qing Feng; Fuwei Luo; Jiansheng Xie
Journal:  J Hum Genet       Date:  2019-08-19       Impact factor: 3.172

10.  ACTG2 variants impair actin polymerization in sporadic Megacystis Microcolon Intestinal Hypoperistalsis Syndrome.

Authors:  Danny Halim; Robert M W Hofstra; Luca Signorile; Rob M Verdijk; Christine S van der Werf; Yunia Sribudiani; Rutger W W Brouwer; Wilfred F J van IJcken; Niklas Dahl; Joke B G M Verheij; Clarisse Baumann; John Kerner; Yolande van Bever; Niels Galjart; Rene M H Wijnen; Dick Tibboel; Alan J Burns; Françoise Muller; Alice S Brooks; Maria M Alves
Journal:  Hum Mol Genet       Date:  2015-12-08       Impact factor: 6.150

View more
  1 in total

1.  Pediatric Intestinal Pseudo-Obstruction: Progress and Challenges.

Authors:  Marie-Catherine Turcotte; Christophe Faure
Journal:  Front Pediatr       Date:  2022-04-13       Impact factor: 3.569

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.