Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero gene.

Abstract

Charcot-Marie-Tooth disease (CMT), or hereditary motor and sensory neuropathy (HMSN), is a clinically and genetically heterogeneous condition. Mutations of the myelin protein zero (MPZ) gene have been associated with CMT1B, Dejerine-Sottas disease, and congenital hypomyelination, which are inherited demyelinating neuropathies characterized by different clinical severity. HMSN type II (HMSN II) or CMT2, the axonal form of CMT, is genetically heterogeneous. Linkage to 1p35-p36 (CMT2A), 3q (CMT2B), and 7p (CMT2D) chromosomes has been reported in the disease; however, most HMSN II families do not link to any of the reported loci. In a large HMSN II Sardinian family, we found a missense mutation in the chromosome 1q MPZ gene. This Ser44Phe mutation was located in exon 2 and was present in the heterozygous state in all affected individuals. This is the first example of an HMSN II family showing an MPZ point mutation. The MPZ gene Ser44Phe mutation found in the HMSN II family presented in this study suggests that genetic analysis of HMSN II families should also include the MPZ gene, previously not considered to be involved in the axonal form of HMSN.

• Authors: M G Marrosu, S Vaccargiu, G Marrosu, A Vannelli, C Cianchetti, F Muntoni
• Journal: Neurology (Neurology) Vol. 50 Issue 5 Pg. 1397-401 (May 1998) ISSN: 0028-3878 [Print] United States
• PMID: 9595994 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Myelin P0 Protein

Topics

• Adult
• Aged
• Charcot-Marie-Tooth Disease (genetics)
• Chromosomes, Human, Pair 17
• Female
• Genetic Linkage
• Humans
• Male
• Middle Aged
• Multigene Family
• Myelin P0 Protein (genetics)
• Pedigree
• Point Mutation
• Sequence Analysis, DNA