Definition

The most common cause of CMT1 is duplication of the PMP22 gene (CMT1A); it disrupts myelin structure, impairing nerve signal transmission and leading to progressive muscle weakness and sensory loss. Variants in the MPZ gene are seen in 5 to 10% of CMT1 cases (CMT1B) and cause similar peripheral nerve damage.

Gene/region examined

MPZ - Exon 1, MPZ - Exon 2, MPZ - Exon 3, MPZ - Exon 4, MPZ - Exon 5, MPZ - Exon 6, MPZ - Exon 7

Method

Sequence analysis

Accepted sample types

EDTA blood, AF, CVS

Inheritance

Hereditary, both autosomal dominant.

Related Tests

Inheritance Patterns

Describes how a genetic condition is passed on within a family. There are five main patterns

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Carrier (Heterozygous / Homozygous)

Why it matters: In autosomal recessive inheritance, when each parent is a carrier (while both appear healthy), the chance of their child being born with the disease is 25% in each

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VUS (Variant of Uncertain Significance)

This is the situation where the test has detected a change in the DNA, but the role of this change in the development of disease is unconfirmed.

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How to Read a Genetic Test Result (Positive / Negative / VUS)

A genetic test result falls into three main categories

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Types of Genetic Tests

A genetic test is a type of medical test that detects changes in genes, chromosomes or proteins. Today there are more than 77,000 genetic tests available.

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