RT Book, Section
A1 Amato, Anthony A.
A1 Russell, James A.
SR Print(0)
ID 1115657906
T1 Charcot–Marie–Tooth Disease and Related Disorders
T2 Neuromuscular Disorders, 2e
YR 2015
FD 2015
PB McGraw-Hill Education
PP New York, NY
SN 9780071752503
LK neurology.mhmedical.com/content.aspx?aid=1115657906
RD 2024/10/11
AB Hereditary  neuropathies  may  account  for  as  many  as  50%  of  previously  undiagnosed  peripheral  neuropathies  referred  to  large  neuromuscular  centers.  Charcot–Marie–Tooth  (CMT)  disease  is  the  most  common  type  of  hereditary  neuropathy,  but,  rather  than  one  disease,  CMT  is  a  syndrome  of  several  genetically  distinct  disorders  (Table  11-1).  In  this  chapter,  we  discuss  CMT  and  related  neuropathies.  In  the  subsequent  chapters,  we  will  review  other  less  common  hereditary  neuropathies  (Chapters  12,  16,  and  30).