Charcot-Marie-Tooth Disease Panel
Charcot-Marie-Tooth Disease Panel
Prezzo di listino
€29.00 EUR
Prezzo di listino
Prezzo scontato
€29.00 EUR
Prezzo unitario
per
Impossibile caricare la disponibilità di ritiro
This product is only meant for customers who already purchased a MyGenome Test
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.
For family planning purposes and for family history of this condition
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
List of main conditions:
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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.
For family planning purposes and for family history of this condition
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 75 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
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
Questo prodotto è destinato esclusivamente ai clienti che hanno già acquistato un test MyGenome