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Myotonic Dystrophy Type 2. DM2 is caused by a defect of the ZNF9 gene on chromosome 3. Myotonic dystrophy DM is a type of muscular dystrophy which is a group of genetic disordersDM is the most common kind of muscular dystrophy in adults.
Myotonic Dystrophy Type 2 Caused By A Cctg Expansion In Intron 1 Of Znf9 Pubmed Ncbi Myotonic Dystrophy The Expanse Protein Kinase from www.pinterest.com
DM2 is an important diagnosis to consider in patients who have proximal muscle weakness around. Myotonic dystrophy type 2 DM2 is characterized by myotonia and muscle dysfunction proximal and axial weakness myalgia and stiffness and less commonly by posterior subcapsular cataracts cardiac conduction defects insulin-insensitive type 2 diabetes mellitus and other endocrine abnormalities. Type 1 myotonic dystrophy is the most common form in most countries.
Myotonic dystrophy type 1 is caused by mutations in the DMPK gene while type 2 results from mutations in the CNBP gene.
The specific defect is a repeat of the cytosine-cytosine-thymine. It is probably more common in central Europe and the USA than the rest of the world. The clinical care of people living with myotonic dystrophy type 2 DM2. Myotonic dystrophy is the most common form of muscular dystrophy that begins in adulthood.
