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Article

Charcot-Marie-Tooth syndrome.

Archives of neurology - 1 Nov 1993

Chance P F, Pleasure D

Abstract excerpt

Charcot-Marie-Tooth syndrome (CMT) is a group of genetically determined symmetric distal polyneuropathies. The CMT loci are known to map to chromosome 1 (CMT1B), chromosome 17 (CMT1A), the X chromosome (CMTX), and two additional unknown autosomes (CMT1C and CMT2). The most prevalent form is CMT1A, an autosomal dominant demyelinative disorder caused either by a tandem duplication in band p11.2-12 of chromosome 17...

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PMID: 8215977
DOI: 10.1001/archneur.1993.00540110060006

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