Charcot-Marie-Tooth disease type 2 subtype D(English)

• caused by defects in the GARS gene, located on chromosome 7, which encodes for glycyl t-RNA synthetase that is involved in protein synthesis in the cell. The symptoms of CMT2D vary in patients, ranging from motor symptoms only, to both sensory and motor symptoms
• CMT2
• Musculoskeletal system, Congenital disorders
• https://charcot…th-type-2-cmt2/