ECE1 Gene Central Hypoventilation Syndrome Congenital Genetic Test
At DNA Labs UAE, we offer the ECE1 Gene Central Hypoventilation Syndrome Congenital Genetic Test at a cost of 4400.0 AED. This test is used to diagnose Central Hypoventilation Syndrome (CHS), also known as Congenital Central Hypoventilation Syndrome (CCHS) or Ondine’s Curse.
Test Components
The ECE1 Gene Central Hypoventilation Syndrome Congenital Genetic Test includes:
- NGS Technology
- Dysmorphology Test Type
- Doctor: Pediatrics
- Test Department: Genetics
Sample Condition
The sample required for this test can be either blood, extracted DNA, or one drop of blood on an FTA Card.
Report Delivery
The report for this test will be delivered within 3 to 4 weeks.
Test Details
The ECE1 gene, also known as the endothelin-converting enzyme 1 gene, is associated with Central Hypoventilation Syndrome (CHS). CHS is a rare genetic disorder that affects the control of breathing, specifically during sleep. Individuals with CHS have difficulty sensing low levels of oxygen and high levels of carbon dioxide in their blood, leading to reduced breathing during sleep.
NGS (Next-Generation Sequencing) Genetic Test is a specialized genetic testing method that analyzes multiple genes simultaneously. In the case of CHS, NGS genetic testing can identify mutations or variations in the ECE1 gene associated with the disorder. This information is crucial for confirming a diagnosis of CHS, predicting disease progression, and guiding treatment options.
It is important to note that NGS genetic testing is a complex procedure that requires expertise in genetic analysis and interpretation. Our specialized laboratory and healthcare professionals have the necessary experience to perform this test accurately.
Pre Test Information
Prior to undergoing the ECE1 Gene Central Hypoventilation Syndrome Congenital Genetic Test, it is recommended to provide the clinical history of the patient who will be tested. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by CHS.
By choosing DNA Labs UAE for your genetic testing needs, you can receive accurate and reliable results for the ECE1 Gene Central Hypoventilation Syndrome Congenital Genetic Test. Our experienced team of healthcare professionals is dedicated to providing the highest quality genetic testing services.
| Test Name | ECE1 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 ECE1 Gene Central hypoventilation syndrome, congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ECE1 Gene Central hypoventilation syndrome, congenital NGS Genetic DNA Test gene ECE1 |
| Test Details |
ECE1 gene, also known as the endothelin-converting enzyme 1 gene, is associated with a rare genetic disorder called Central Hypoventilation Syndrome (CHS), or more commonly known as Congenital Central Hypoventilation Syndrome (CCHS) or Ondine’s Curse. CHS is a disorder that affects the control of breathing, specifically during sleep. Individuals with CHS have difficulty sensing low levels of oxygen and high levels of carbon dioxide in their blood, which leads to hypoventilation (reduced breathing) during sleep. However, their breathing remains normal during wakefulness and voluntary control. NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of CHS, NGS genetic testing can be used to identify mutations or variations in the ECE1 gene that are associated with the disorder. By performing NGS genetic testing, healthcare professionals can confirm a diagnosis of CHS and identify the specific genetic mutation causing the disorder. This information is important for genetic counseling, predicting disease progression, and potentially guiding treatment options for individuals with CHS. It is worth noting that NGS genetic testing is a complex and specialized procedure that requires expertise in genetic analysis and interpretation. It is typically performed by specialized laboratories and healthcare professionals with experience in genetic testing and genetic disorders. |
