Literature DB >> 25573720

Gastrointestinal problems in 15q duplication syndrome.

Elias A Shaaya1, Sarah F Pollack1, Susana Boronat1, Shelby Davis-Cooper1, Garrett C Zella2, Ronald L Thibert3.   

Abstract

Chromosome 15q duplication syndrome (Dup15q syndrome) is a neurodevelopmental disorder involving copy number gains of the maternal chromosome 15q11.2-q13 region, characterized by intellectual disability, developmental delay, autism spectrum disorder (ASD), and epilepsy. Gastrointestinal (GI) problems in Dup15q syndrome have been reported only rarely, mostly focused on neonatal feeding difficulties. A retrospective review of the medical records of 46 patients with Dup15q syndrome was conducted to assess GI issues and their treatments in this population. GI symptoms were present in 76.7% of subjects with an isodicentric duplication and 87.5% with an interstitial duplication. There was no clear association between GI issues and ASD, with symptoms occurring in 78.9% of all subjects and 78.2% of ASD subjects. The most commonly reported symptoms were gastroesophageal reflux (56.7%) and constipation (60%), with 30% of subjects reporting both. The most common treatments were polyethylene glycol for constipation and proton pump inhibitors for reflux. Behaviors such as irritability and aggressiveness improved with treatment of GI symptoms in several subjects. The results indicate that GI symptoms are common in Dup15q syndrome and may have an atypical presentation. Diagnosis may be difficult, especially in individuals who are nonverbal or minimally verbal, so increased awareness is critical for early diagnosis and treatment.
Copyright © 2015 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  15q duplication syndrome; Constipation; Dup15q; GI; GI reflux

Mesh:

Substances:

Year:  2015        PMID: 25573720     DOI: 10.1016/j.ejmg.2014.12.012

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  4 in total

1.  Early Indicators of Creatine Transporter Deficiency.

Authors:  Judith S Miller; Rebecca P Thomas; Amanda Bennett; Simona Bianconi; Aleksandra Bruchey; Robert J Davis; Can Ficicioglu; Whitney Guthrie; Forbes D Porter; Audrey Thurm
Journal:  J Pediatr       Date:  2018-12-20       Impact factor: 4.406

Review 2.  [Genetic findings in autism spectrum disorders].

Authors:  C M Freitag
Journal:  Nervenarzt       Date:  2017-07       Impact factor: 1.214

3.  Case Report: Autism Risk Within the Context of Two Chromosome 15 Syndromes.

Authors:  Ashleigh M Kellerman; Mehreen Z Hassan; Emily A Abel; Molly Reilly; Rebecca McNally Keehn; A J Schwichtenberg
Journal:  J Autism Dev Disord       Date:  2022-01-07

Review 4.  The Gut-Brain-Microbiome Axis and Its Link to Autism: Emerging Insights and the Potential of Zebrafish Models.

Authors:  David M James; Elizabeth A Davidson; Julio Yanes; Baharak Moshiree; Julia E Dallman
Journal:  Front Cell Dev Biol       Date:  2021-04-15
  4 in total

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