Dystrophia myotonica in a 47, XXY male

Miguel E. Fiol, Richard F. Daly, Richard H. Osborne

Research output: Contribution to journalArticle

6 Scopus citations

Abstract

Classical clinical manifestations of dystrophia myotonica were apparently unaltered by aneuploidy in a 47.XXY male. His extremely eunuchoid habitus may represent a contribution by the point mutation to his Klinefelter’s syndrome. Association of the two disorders may be due to factors other than chance. The danger of overlooking Klinefelter’s syndrome in males with dystrophia myotonica can be avoided by cytologic studies.

Original languageEnglish (US)
Pages (from-to)472-476
Number of pages5
JournalNeurology
Volume25
Issue number5
StatePublished - May 1975
Externally publishedYes

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    Fiol, M. E., Daly, R. F., & Osborne, R. H. (1975). Dystrophia myotonica in a 47, XXY male. Neurology, 25(5), 472-476.