This Article  • References  • Full text PDF  • Reply to article  • Send to a friend  • Save in My Folder  • Save to citation manager  • Permissions  Citing Articles  • Contact me when this article is cited  Related Content  • Similar articles in this journal  Social Bookmarking   What's this?

G. B. A. Duchenne; de Boulogne

Arch Neurol. 1968;19(6):629-636.

	Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

A. Definition and Naming of the Disease The disease I will describe is characterized principally by: (1) weakness of movements, usually settling at first in the muscles of the lower extremities and the lumbar spine, then spreading to the upper extremities at the terminal stage and worsening at the same time until movement is abolished; (2) increase of volume either (ordinarily) in several of the paralyzed muscles or (exceptionally) in nearly all the paralyzed muscles; (3) hyperplasia of the interstitial connettive tissue of the paralyzed muscles, with an abundant production of fibrous tissue or of fatty vesicles in the more advanced stage.

I propose to call this disease pseudohyper-trophic muscular paralysis after its principal objective clinical signs or myosclerotic paralysis after its peripheral anatomic characteristics. These terms will be justified by studying the symptomatology and the pathologic anatomy in the living during the course of the disease. I prefer . . . [Full Text PDF of this Article]

Footnotes
Translation of: Recherches sur la paralysie musculaire pseudo-hypertrophique, ou paralysie myosclérosique, Archives Générales de Médecine 11:5-25, 179-209, 305-321, 421-443, 552-588, 1868.

Electrisation localisée, 2e edition, 1861, paraplégie hypertrophique congénitale, p. 364.

CiteULike    Connotea    Del.icio.us    Digg    Reddit    Technorati    Twitter     What's this?