Literature DB >> 30921255

Incontinence in Phelan-McDermid Syndrome.

Claire Witmer1,2, Aviva Mattingly2, Precilla DʼSouza3, Audrey Thurm3, Colleen Hadigan2.   

Abstract

OBJECTIVE: The aim of the study was to evaluate gastrointestinal symptoms and continence in the context of Phelan-McDermid Syndrome (PMS).
METHODS: A prospective evaluation of children with PMS (n = 17) at the National Institutes of Health.
RESULTS: Parent-reported history of symptoms were common: constipation (65%), reflux (59%), choking/gagging (41%), and more than half received gastrointestinal specialty care. No aspiration was noted in 11/11 participants who completed modified barium swallows. Four participants met criteria for functional constipation, 2 of whom had abnormal colonic transit studies. Stool incontinence was highly prevalent (13/17) with nonretentive features present in 12/17. Participants who were continent had significantly smaller genetic deletions (P = 0.01) and higher nonverbal mental age (P = 0.03) compared with incontinent participants.
CONCLUSIONS: Incontinence is common in PMS and associated with intellectual functioning and gene deletion size. Management strategies may differ based on the presence of nonretentive fecal incontinence, functional constipation, and degree of intellectual disability for children with PMS.

Entities:  

Mesh:

Year:  2019        PMID: 30921255      PMCID: PMC6658348          DOI: 10.1097/MPG.0000000000002342

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  16 in total

1.  Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.

Authors:  Christelle M Durand; Catalina Betancur; Tobias M Boeckers; Juergen Bockmann; Pauline Chaste; Fabien Fauchereau; Gudrun Nygren; Maria Rastam; I Carina Gillberg; Henrik Anckarsäter; Eili Sponheim; Hany Goubran-Botros; Richard Delorme; Nadia Chabane; Marie-Christine Mouren-Simeoni; Philippe de Mas; Eric Bieth; Bernadette Rogé; Delphine Héron; Lydie Burglen; Christopher Gillberg; Marion Leboyer; Thomas Bourgeron
Journal:  Nat Genet       Date:  2006-12-17       Impact factor: 38.330

2.  The normal range and a simple diagram for recording whole gut transit time.

Authors:  R C Evans; M A Kamm; J M Hinton; J E Lennard-Jones
Journal:  Int J Colorectal Dis       Date:  1992-02       Impact factor: 2.571

3.  A parent training model for toilet training children with autism.

Authors:  K Kroeger; R Sorensen
Journal:  J Intellect Disabil Res       Date:  2010-06

4.  Clinical and genomic evaluation of 201 patients with Phelan-McDermid syndrome.

Authors:  Sara M Sarasua; Luigi Boccuto; Julia L Sharp; Alka Dwivedi; Chin-Fu Chen; Jonathan D Rollins; R Curtis Rogers; Katy Phelan; Barbara R DuPont
Journal:  Hum Genet       Date:  2014-01-31       Impact factor: 4.132

5.  The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome).

Authors:  K Phelan; H E McDermid
Journal:  Mol Syndromol       Date:  2011-11-22

6.  Development of bowel and bladder control in the mentally retarded.

Authors:  L von Wendt; S Similä; P Niskanen; M R Järvelin
Journal:  Dev Med Child Neurol       Date:  1990-06       Impact factor: 5.449

Review 7.  Colonic transit studies: normal values for adults and children with comparison of radiological and scintigraphic methods.

Authors:  Bridget R Southwell; Melanie C C Clarke; Jonathan Sutcliffe; John M Hutson
Journal:  Pediatr Surg Int       Date:  2009-06-02       Impact factor: 1.827

Review 8.  Urinary incontinence in children with special needs.

Authors:  Alexander von Gontard
Journal:  Nat Rev Urol       Date:  2013-10-01       Impact factor: 14.432

Review 9.  Phelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoring.

Authors:  Alexander Kolevzon; Benjamin Angarita; Lauren Bush; A Ting Wang; Yitzchak Frank; Amy Yang; Robert Rapaport; Jeffrey Saland; Shubhika Srivastava; Cristina Farrell; Lisa J Edelmann; Joseph D Buxbaum
Journal:  J Neurodev Disord       Date:  2014-10-08       Impact factor: 4.025

10.  Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.

Authors:  Latha Soorya; Alexander Kolevzon; Jessica Zweifach; Teresa Lim; Yuriy Dobry; Lily Schwartz; Yitzchak Frank; A Ting Wang; Guiqing Cai; Elena Parkhomenko; Danielle Halpern; David Grodberg; Benjamin Angarita; Judith P Willner; Amy Yang; Roberto Canitano; William Chaplin; Catalina Betancur; Joseph D Buxbaum
Journal:  Mol Autism       Date:  2013-06-11       Impact factor: 7.509

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  1 in total

1.  Shank promotes action potential repolarization by recruiting BK channels to calcium microdomains.

Authors:  Luna Gao; Jian Zhao; Evan Ardiel; Qi Hall; Stephen Nurrish; Joshua M Kaplan
Journal:  Elife       Date:  2022-03-10       Impact factor: 8.713

  1 in total

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