| Literature DB >> 22848312 |
Hetal Pandya1, Jitendra Lakhani, Jigar Mehta, Jimmy Dodhania.
Abstract
Myotonic dystrophy is also known as dystrophia myotonica (DM). The condition is composed of at least two clinical disorders with overlapping phenotypes and distinct molecular genetic defects: myotonic dystrophy type 1, the classic disease originally described by Steinert, and myotonic dystrophy type 2, also called proximal myotonic myopathy (PROMM). Mega cisterna magna is thought to be an anatomic variant with no clinical significance. We report a rare case of type 1 dystrophia myotonica in combination with mega cisterna magna.Entities:
Keywords: Dystrophia myotonica; congenital myotonic dystrophy; mega cisterna magna
Year: 2012 PMID: 22848312 PMCID: PMC3395281 DOI: 10.4066/AMJ.2012.1000
Source DB: PubMed Journal: Australas Med J ISSN: 1836-1935