Cholestasis and Myotonic Dystrophy
- 9 August 1979
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 301 (6) , 329-330
- https://doi.org/10.1056/nejm197908093010613
Abstract
To the Editor: Myotonic dystrophy (Steinert's disease) is an uncommon disorder of unknown cause, with involvement of smooth and striated muscle.1 We have observed an unusual manifestation, anicteric cholestasis, in two patients with this disease.A 49-year-old woman was admitted to the hospital after reporting weakness of the limbs. The diagnosis of myotonic dystrophy was made on clinical, electrophysiologic and histologic grounds. There was no alcoholism, no drug intake and no pruritus. The liver and the spleen were not palpable; there were no clinical features of hepatocellular failure or portal hypertension. The total bilirubin level was 0.6 mg per 100 . . .Keywords
This publication has 6 references indexed in Scilit:
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- Anal Sphincter Abnormalities Characteristic of Myotonic DystrophyGastroenterology, 1965
- ABNORMALITIES IN SWALLOWING ASSOCIATED WITH DYSTROPHIA MYOTONICABrain, 1965
- Unusual Manifestations Due to Involvement of Involuntary Muscle in Dystrophia MyotonicaNew England Journal of Medicine, 1964