EDN3 Gene Central Hypoventilation Syndrome Congenital Genetic Test
Are you or your loved one experiencing symptoms of Central Hypoventilation Syndrome (CHS)? DNA Labs UAE offers a comprehensive genetic test to diagnose this rare autosomal dominant disorder. Our EDN3 Gene Central Hypoventilation Syndrome Congenital Genetic Test can provide valuable information for patients and their families.
Test Name: EDN3 Gene Central Hypoventilation Syndrome Congenital Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
Report Delivery: 3 to 4 Weeks
Method: NGS Technology
Test type: Dysmorphology
Doctor: Pediatrics
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for EDN3 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EDN3 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test gene EDN3
About EDN3 Gene and Central Hypoventilation Syndrome (CHS)
The EDN3 gene, also known as endothelin 3 gene, is associated with a genetic disorder called Central Hypoventilation Syndrome (CHS), also known as Congenital Central Hypoventilation Syndrome (CCHS) or Ondine’s Curse. CHS is a rare autosomal dominant disorder that affects the control of breathing.
Next-generation sequencing (NGS) genetic testing is a powerful tool used to analyze multiple genes simultaneously, allowing for a comprehensive evaluation of genetic variants associated with a particular disorder. In the case of CHS, NGS genetic testing can be used to identify variants in the EDN3 gene that may be responsible for the syndrome.
NGS genetic testing involves sequencing the DNA of an individual to identify specific genetic variants. In the context of CHS, the EDN3 gene is sequenced to identify any mutations or variants that may be present. These variants can help diagnose CHS and provide valuable information for genetic counseling and management of the condition.
It is important to note that while NGS genetic testing can be helpful in diagnosing CHS, it is not the only diagnostic tool. Clinical evaluation, family history, and other diagnostic tests may also be necessary to confirm the diagnosis of CHS.
Overall, NGS genetic testing of the EDN3 gene can aid in the diagnosis and management of Central Hypoventilation Syndrome, providing valuable information for patients and their families.
| Test Name | EDN3 Gene Central hypoventilation syndrome congenital Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Dysmorphology |
| Doctor | Pediatrics |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for EDN3 Gene Central hypoventilation syndrome, congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EDN3 Gene Central hypoventilation syndrome, congenital NGS Genetic DNA Test gene EDN3 |
| Test Details |
EDN3 gene, also known as endothelin 3 gene, is associated with a genetic disorder called Central Hypoventilation Syndrome (CHS), also known as Congenital Central Hypoventilation Syndrome (CCHS) or Ondine’s Curse. CHS is a rare autosomal dominant disorder that affects the control of breathing. Next-generation sequencing (NGS) genetic testing is a powerful tool used to analyze multiple genes simultaneously, allowing for a comprehensive evaluation of genetic variants associated with a particular disorder. In the case of CHS, NGS genetic testing can be used to identify variants in the EDN3 gene that may be responsible for the syndrome. NGS genetic testing involves sequencing the DNA of an individual to identify specific genetic variants. In the context of CHS, the EDN3 gene is sequenced to identify any mutations or variants that may be present. These variants can help diagnose CHS and provide valuable information for genetic counseling and management of the condition. It is important to note that while NGS genetic testing can be helpful in diagnosing CHS, it is not the only diagnostic tool. Clinical evaluation, family history, and other diagnostic tests may also be necessary to confirm the diagnosis of CHS. Overall, NGS genetic testing of the EDN3 gene can aid in the diagnosis and management of Central Hypoventilation Syndrome, providing valuable information for patients and their families. |
