Postoperative complications of dystrophia myotonica

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چکیده

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Respiration in Dystrophia Myotonica.

The interesting paper by Dr J E Clague et al (March 1994;49:240-4) contains some results and conclusions which are at variance with earlier studies. Firstly, their results showed that the vent-ilatory response to carbon dioxide in these patients was lower than in the controls, but the difference was not significant. Several earlier studies showed clear evidence of a reduction in the slope of th...

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Electrophysiological study of dystrophia myotonica.

A comprehensive electrophysiological study has been made of the extensor digitorum brevis muscle and its motor innervation in 17 patients with dystrophia myotonica. The mean contraction and half-relaxation times were prolonged in the isometric twitches of dystrophic muscles. Decremental responses to repetitive motor nerve stimulation were found in two patients. All the terminal latency measurem...

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Dystrophia myotonica: a multisystem disease.

AN AI~A~S'rHESIOLOCIST is aware of the need for caution when confronted with a patient suffering from a myotonic syndrome. On reviewing the literature, 1,2 it becomes evident that the stress has been on the myotonic aspects of the disease. However, dystrophia myotonica is a multisystem disease, and the following case report and related discussion illustrate the many facets which need considerat...

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Serum insulin, blood sugar, and growth hormone levels were measured in response to a 50g oral glucose tolerance test in 10 patients with proven dystrophia myotonica. Three patients belonged to one family; seven patients had no known family history of the disease. One patient, a chronic invalid aged 56 years, produced a mild diabetic glucose tolerance curve and a delayed prolonged rise in serum ...

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ژورنال

عنوان ژورنال: Anaesthesia

سال: 1987

ISSN: 0003-2409,1365-2044

DOI: 10.1111/j.1365-2044.1987.tb05398.x