Search Results for: cmt

…that can cause type 2 include: CMT2A, CMT2A2B, CMT2B4, HMSN6A – Mitofusin 2 (MFN2) CMT2B – Members RAS oncogene family (RAB7 or RAB7A) CMT2B1 – Lamin A/C (LMNA) CMT2B2 –…

Charcot-Marie-Tooth disease Type 1 (CMT1) What is CMT Type 1? CMT Type 1 (CMT1) is defined as an autosomal dominant (see inheritance) demyelinating form of CMT. CMT1 accounts for about…

…of autosomal dominant CMT Type 2T, characterized by late-onset axonal CMT, usually starting around age 50. Finally, I knew—2T. Four generations of my family have had CMT symptoms consistent with…