Intern. Med. volume 35, issue 9, P746-748 1996 DOI: 10.2169/internalmedicine.35.746 View full text
Takuya KOMENO, Haruhiko NINOMIYA, Takayoshi ITOH, Tsuneo FUJITA, Toshiro NAGASAWA, Tsukasa ABE

Abstract: Hemolytic anemia developed in a male who had been diagnosed as having myotonic muscular dystrophy (MMD). His red cell life-span examined by 51Cr-labeling method was shortened (T1/2 = 6.5 days). Specific abnormalities of red cells were not found other than increased osmotic resistance, increased intracellular sodium, and decreased intracellular potassium of red cells. A clinical review of 18 other patients with MMD did not reveal any signs ofhemolysis. It may be suggested that the underlying red cell membraned…

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