Marfan Syndrome Panel
Marfan Syndrome Panel
Normaler Preis
€29.00 EUR
Normaler Preis
Verkaufspreis
€29.00 EUR
Grundpreis
pro
Verfügbarkeit für Abholungen konnte nicht geladen werden
This product is only meant for customers who already purchased a MyGenome Test
Marfan syndrome is a genetic condition that affects the connective tissue, which provides support to the body and organs. Marfan syndrome can damage blood vessels, the heart, eyes, skin, lungs, and bones in the hips, spine, feet, and rib cage.
Marfan syndrome is a genetic disorder that affects the connective tissue of the body and can cause a variety of symptoms, including skeletal abnormalities, cardiovascular complications, and vision problems. Marfan syndrome is caused by mutations in the fibrillin-1 (FBN1) gene, and this panel tests for genetic variants that are known to affect this gene.
This panel is designed for individuals with a family history of Marfan syndrome or individuals with symptoms of the condition, such as a tall and slender build, scoliosis, and heart murmur. 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:
Vollständige Details anzeigen
Marfan syndrome is a genetic condition that affects the connective tissue, which provides support to the body and organs. Marfan syndrome can damage blood vessels, the heart, eyes, skin, lungs, and bones in the hips, spine, feet, and rib cage.
Marfan syndrome is a genetic disorder that affects the connective tissue of the body and can cause a variety of symptoms, including skeletal abnormalities, cardiovascular complications, and vision problems. Marfan syndrome is caused by mutations in the fibrillin-1 (FBN1) gene, and this panel tests for genetic variants that are known to affect this gene.
This panel is designed for individuals with a family history of Marfan syndrome or individuals with symptoms of the condition, such as a tall and slender build, scoliosis, and heart murmur. 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 25 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Marfan Syndrome
Dieses Produkt ist nur für Kunden gedacht, die bereits einen MyGenome-Test erworben haben.