
Clinico-Electrophysiological and genetic overlaps and magnetic resonance imaging findings in Charcot–Marie– Tooth disease: A pilot study from Western India
Author(s) -
Satish V. Khadilkar,
Nahush D Patil,
N. Kadam,
Khushnuma A Mansukhani,
Bhagyadhan A. Patel
Publication year - 2017
Publication title -
annals of indian academy of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.427
H-Index - 31
eISSN - 1998-3549
pISSN - 0972-2327
DOI - 10.4103/aian.aian_316_17
Subject(s) - medicine , magnetic resonance neurography , genetic testing , magnetic resonance imaging , concordance , pathology , radiology
Charcot-Marie-Tooth (CMT) disease is clinically and genetically heterogeneous. There are no published series describing clinical, electrophysiological, and genetic information on CMT from the Indian subcontinent. Magnetic resonance imaging (MRI) neurography technique provides useful information about the plexus and roots and can be employed in patients with CMT.