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Acta Ortop Mex. 2008 Jul-Aug;22(4):268-77.

[Diagnosis of the peripheral hereditary neuropathies and its molecular genetics].

[Article in Spanish]

Author information

1
Servicio de Genética, Instituto Nacional de Rehabilitación, Av. México-Xochimilco Núm, 289, Arenal de Guadalupe, Tlalpan C.P. 14389, DF México. edghernandez@inr.gob.mx

Abstract

Peripheral neuropathies include a wide range of pathological disorders characterized by damage of peripheral nerves. Among them, peripheral hereditary neuropathies are a group of frequent illnesses and early evolution. They have been named hereditary motor and sensory neuropathy (HMSN) or peripheral hereditary neuropathies type Charcot-Marie-Tooth (CMT). The most frequent types are CMT1, CMT2 and CMTX. Approximately 70% of the cases correspond to subtype CMT1A, associated with tandem duplication of a 1.5 Mb DNA fragment on chromosome 17p11.2-p12 that codifies the peripheral myelin protein PMP22. So far, there five different types of CMT (1,2,3,4,X) with approximately 32 subtypes, associated with more than 30 genes. Have been reported genetic heterogeneity and expression variability of the illness makes it necessary to carry on diagnostic strategies that integrate clinical study for determining genetic clinical history, family history, complete physical exploration, muscular strength, physical deformities, reflexes and sensitivity, and molecular studies allow detection of different types of mutations and help establish a correct diagnosis and an adequate genetic counseling.

PMID:
18979992
[Indexed for MEDLINE]
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