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Gastrointestinal Dysmotility Is a Significant Feature in 2 Siblings With a Novel Inositol 1,4,5-Triphosphate Receptor 1 ( ITPR1 ) Missense Variant.

Authors :
Butler Tjaden NE
Chiou EH
Pillai NR
Schady DA
Chumpitazi BP
Source :
ACG case reports journal [ACG Case Rep J] 2021 Oct 26; Vol. 8 (10), pp. e00676. Date of Electronic Publication: 2021 Oct 26 (Print Publication: 2021).
Publication Year :
2021

Abstract

We present 2 siblings with a novel type 1 inositol 1,4,5-triphosphate receptor ( ITPR1 ) missense variant who exhibit gastrointestinal dysmotility (chronic constipation and gastroparesis). ITPR1 is expressed in the cerebellum and interstitial cells of Cajal. Periodic release of calcium by ITPR1 initiates pacemaker currents, resulting in smooth muscle contraction. ITPR1 mutations are known to be associated with neurologic syndromes, and these variants have not previously been associated with significant gastrointestinal manifestations in humans. Using whole-genome sequencing, in silico prediction software, biopsy samples, and manometry, the identified novel ITPR1 variant is likely pathogenic and may have neurogastroenterology implications.<br /> (© 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology.)

Details

Language :
English
ISSN :
2326-3253
Volume :
8
Issue :
10
Database :
MEDLINE
Journal :
ACG case reports journal
Publication Type :
Report
Accession number :
34722792
Full Text :
https://doi.org/10.14309/crj.0000000000000676