## ABSTRACT Three cases of androgenβdependent disease in females with myotonic dystrophy are described. Serum androgens in individuals affected by myotonic dystrophy are known to be lower on average than in normal controls. Despite this these three females developed diseases that are androgen depen
A case of myotonic dystrophy associated with SIADH
β Scribed by A. Tamaoka; Y. Nishimura
- Publisher
- Springer
- Year
- 1987
- Tongue
- English
- Weight
- 243 KB
- Volume
- 234
- Category
- Article
- ISSN
- 0340-5354
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Length of (CTG)n triplet repeats in myotonic dystrophy protein kinase gene (DMPK) was estimated in tumors, normal tissues of the same organs, muscles, and leukocytes from three myotonic dystrophy (DM) patients and a non-DM patient. Using cDNA 25 as a probe, a Southern blot analysis of EcoRI- and Bgl
## Communicated by Alan Malcolm Myotonic dystrophy (DM) is an adult form of muscular dystrophy affecting about 1 in 8,000 individuals in most populations. Although common symptoms include progressive muscle weakness and stiffness, it is characterised by a heterogenous clinical picture. Despite thi