Fanconi Anemia Panel
Fanconi Anemia Panel
Prix habituel
€29.00 EUR
Prix habituel
Prix soldé
€29.00 EUR
Prix unitaire
par
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This product is only meant for customers who already purchased a MyGenome Test
Fanconi anemia is a condition that affects many parts of the body. People with this condition may have bone marrow failure, physical abnormalities, organ defects, and an increased risk of certain types of cancer.
Fanconi anemia is a rare inherited disorder that affects bone marrow function and increases the risk of developing certain types of cancer, such as leukemia. Fanconi anemia is caused by mutations in genes involved in DNA repair and cell cycle regulation.
This panel is designed for individuals with a family history of Fanconi anemia or individuals with symptoms of the condition, such as abnormal blood counts or birth defects. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members.
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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Fanconi anemia is a condition that affects many parts of the body. People with this condition may have bone marrow failure, physical abnormalities, organ defects, and an increased risk of certain types of cancer.
Fanconi anemia is a rare inherited disorder that affects bone marrow function and increases the risk of developing certain types of cancer, such as leukemia. Fanconi anemia is caused by mutations in genes involved in DNA repair and cell cycle regulation.
This panel is designed for individuals with a family history of Fanconi anemia or individuals with symptoms of the condition, such as abnormal blood counts or birth defects. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members.
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 20 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Fanconi Anemia
Ce produit est uniquement destiné aux clients qui ont déjà acheté un test MyGenome.