Charcot-Marie-Tooth Disease Report
Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth is a genetically complex disease, which can be transmitted in an autosomal dominant, recessive and X-linked manner. The underlying mutations, which can affect multiple genes, affect the functions of the peripheral nerves of the legs, feet and hands, causing sensory and motor neuropathies, with serious consequences on the transmission of nerve impulses to the muscles.
More than 75 genes analyzed
It is recommended if:
For family planning purposes and for family history of this condition
List of main conditions:
- Charcot-Marie-Tooth disease axonal type 2n
- Charcot-Marie-Tooth Disease, Type 4H
- Neuropathy, Hereditary Sensory And Autonomic
- Charcot-Marie-Tooth Disease, Dominant Intermediate C
Simple workflow
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