Glucocorticoid Deficiency Panel
€29.00
/
This product is only meant for customers who already purchased a Dante Genome Test
The genetic variants analyzed in this panel are closely related to or potentially the cause of serious glucocorticoid deficiency conditions
Glucocorticoid deficiency is a rare disorder that affects the body's production of cortisol, a hormone involved in stress response. Glucocorticoid deficiency is caused by mutations in genes involved in the regulation of cortisol production, and this panel tests for genetic variants that are known to affect these processes.
This panel is designed for individuals with a family history of glucocorticoid deficiency or individuals with symptoms of the condition, such as fatigue, weakness, and hypoglycemia. 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:
The genetic variants analyzed in this panel are closely related to or potentially the cause of serious glucocorticoid deficiency conditions
Glucocorticoid deficiency is a rare disorder that affects the body's production of cortisol, a hormone involved in stress response. Glucocorticoid deficiency is caused by mutations in genes involved in the regulation of cortisol production, and this panel tests for genetic variants that are known to affect these processes.
This panel is designed for individuals with a family history of glucocorticoid deficiency or individuals with symptoms of the condition, such as fatigue, weakness, and hypoglycemia. 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 10 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Lipoid adrenal hyperplasia,
- Achalasia-addisonianism-alacrimia syndrome
- Glucocorticoid deficiency, due to ACTH unresponsiveness
Our certifications
