Acute Gastroparesis in Duchenne's Muscular Dystrophy

Byung Chun Chung; Hyo Jin Park; Seung Baik Yoon; Hong Woo Lee; Ki Whang Kim; Sang In Lee; In Suh Park

doi:10.3349/ymj.1998.39.2.175

Acute Gastroparesis in Duchenne's Muscular Dystrophy

Byung Chun Chung, Hyo Jin Park, Seung Baik Yoon, Hong Woo Lee, Ki Whang Kim, Sang In Lee, In Suh Park

Department of Internal Medicine

Research output: Contribution to journal › Article › peer-review

15 Citations (Scopus)

Abstract

Duchenne's muscular dystrophy(DMD) is an X-linked recessive disease. Clinical descriptions of the disorder focus principally on skeletal muscle degeneration. Another manifestation, which involves the gastrointestinal tract, may be fatal. But its prevalence remains undefined. We report here a case of acute gastroparesis associated with Duchenne's muscular dystrophy. In our case, the patient's symptoms were improved by prokinetic agents and timely decompression in life-threatening acute gastric dilatation.

Original language	English
Pages (from-to)	175-179
Number of pages	5
Journal	Yonsei medical journal
Volume	39
Issue number	2
DOIs	https://doi.org/10.3349/ymj.1998.39.2.175
Publication status	Published - 1998

All Science Journal Classification (ASJC) codes

Medicine(all)

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title = "Acute Gastroparesis in Duchenne's Muscular Dystrophy",

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AU - Chung, Byung Chun

AU - Park, Hyo Jin

AU - Yoon, Seung Baik

AU - Lee, Hong Woo

AU - Kim, Ki Whang

AU - Lee, Sang In

AU - Park, In Suh

PY - 1998

Y1 - 1998

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AB - Duchenne's muscular dystrophy(DMD) is an X-linked recessive disease. Clinical descriptions of the disorder focus principally on skeletal muscle degeneration. Another manifestation, which involves the gastrointestinal tract, may be fatal. But its prevalence remains undefined. We report here a case of acute gastroparesis associated with Duchenne's muscular dystrophy. In our case, the patient's symptoms were improved by prokinetic agents and timely decompression in life-threatening acute gastric dilatation.

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Acute Gastroparesis in Duchenne's Muscular Dystrophy

Abstract

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