CMTX


Also found in: Medical.
AcronymDefinition
CMTXCharcot-Marie-Tooth Disease, X-Linked
References in periodicals archive ?
Here, we reported nine Chinese families with CMTX and identified three novel GJB1 point mutations in three unrelated families.
Disease Pathology Inheritance Genes/chromosomal name (a) mode loci associated with disease, n CMT1 Abnormal myelin AD (b) 9 CMT2 Axonopathy AD 19 CMT4 Either myelinopathy AR 10 or axonopathy CMTX Axonopathy with XLD 2 secondary myelin changes Disease Proportion name (a) of all CMT, % CMT1 40-50 CMT2 10-15 CMT4 Rare CMTX 10-15 (a) Intermediate dominant (dominant inheritance with NCV between demylinating and axonopathic) and other rare forms are not included.
9) CMT sub-type, n (%) CMT1A 11 (73) 11 (73) CMTX 4 (27) 1 (7) Dejerine-Sottas syndrome 0 (0) 1 (7) Spinal CMT 0 (0) 1 (7) CMT2 0 (0) 1 (7) CMT = Charcot-Marie-Tooth disease, Exp = experimental group, Con = control group Table 2.