Sigmoid Volvulus in Myotonic Dystrophy Type I (Steinert Disease)

Myotonic dystrophy (MD) is a progressive multisystem genetic disorder that is characterized by progressive muscle weakness and wasting. MD1 (also known as Steinert disease) is associated with various clinical entities such as skeletal muscle weakness, myotonia, cardiac abnormalities, respiratory dys...

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Bibliographic Details
Main Authors: Ahmed B. Bayoumy, Jennifer Suzanne Gjertsen, Maarten E. Tushuizen
Format: Article
Language:English
Published: Karger Publishers 2022-03-01
Series:Case Reports in Gastroenterology
Subjects:
Online Access:https://www.karger.com/Article/FullText/522476
Description
Summary:Myotonic dystrophy (MD) is a progressive multisystem genetic disorder that is characterized by progressive muscle weakness and wasting. MD1 (also known as Steinert disease) is associated with various clinical entities such as skeletal muscle weakness, myotonia, cardiac abnormalities, respiratory dysfunction, gastrointestinal involvement, and cognitive impairment. In this case report, we present a 32-year-old woman with MD1 who presented with a sigmoid volvulus, which was treated with endoscopic decompression.
ISSN:1662-0631