The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major endocrinological conditions
Endocrinology panel is used to identify genetic variants associated with endocrine disorders, which affect the body's hormone-producing glands, such as the thyroid, pancreas, and pituitary gland. Endocrine disorders can cause a wide range of symptoms, depending on the specific condition. This panel tests for genetic variants that are known to affect hormone production and signaling, as well as genes involved in metabolic function.
This panel is designed for individuals with a family history of endocrine disorders or individuals with symptoms of the conditions, such as unexplained weight gain or fatigue. 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 220 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Congenital Hypothyroidism
- Aromatase Deficiency
- Congenital leptin deficiency
- Hypoplastic Pancreas-Intestinal
- Atresia-Hypoplastic Gallbladder Syndrome
Dieses Produkt ist nur für Kunden gedacht, die bereits einen MyGenome-Test erworben haben.