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Congenital Adrenal Hyperplasia Panel NGS Genetic Test

Original price was: 6,000 د.إ.Current price is: 4,400 د.إ.

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The Congenital Adrenal Hyperplasia (CAH) Panel NGS Genetic Test is a comprehensive diagnostic tool offered by DNA Labs UAE, designed to identify genetic mutations associated with CAH, a group of inherited disorders affecting the adrenal glands. This next-generation sequencing (NGS) test analyzes multiple genes known to be involved in the condition, providing a detailed assessment of genetic variations that could lead to CAH. By pinpointing specific genetic mutations, the test facilitates early and accurate diagnosis, allowing for personalized treatment plans and management strategies to be developed. The test is priced at 4400 AED, reflecting the advanced technology and expertise required to perform this sophisticated genetic analysis. Through early detection and intervention, individuals with CAH can lead healthier lives, making this test a valuable resource for those at risk or exhibiting symptoms of the disorder.

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  • This test is not intended for medical diagnosis or treatment
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Congenital Adrenal Hyperplasia Panel NGS Genetic Test

At DNA Labs UAE, we offer the Congenital Adrenal Hyperplasia Panel NGS Genetic DNA Test at a cost of AED 4400.0. This test is used to diagnose and determine the severity of Congenital Adrenal Hyperplasia (CAH), a group of inherited disorders affecting the adrenal glands.

Test Details

CAH can cause abnormal development of the genitals, early puberty, and other health problems. Our Congenital Adrenal Hyperplasia Panel NGS Genetic DNA Test analyzes a person’s DNA to identify mutations in genes associated with CAH. Using next-generation sequencing (NGS) technology, we read the entire genetic code of these genes, allowing for a more comprehensive analysis compared to traditional genetic tests.

Benefits of the Test

The results of the Congenital Adrenal Hyperplasia Panel NGS Genetic DNA Test can help diagnose CAH, determine the type and severity of the condition, and inform treatment decisions. Additionally, the test can identify carriers of CAH mutations, which is useful for family planning.

Test Process

The test requires a blood or saliva sample, which can be provided by the patient. A healthcare provider must order the test, and the results are usually available within three to four weeks.

Pre-Test Information

Prior to undergoing the Congenital Adrenal Hyperplasia Panel NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by genes such as CYP11A1, CYP11B1, CYP17A1, CYP21A2, HSD3B2, POR, PRKAR1A, and STAR.

Conclusion

If you suspect Congenital Adrenal Hyperplasia or have a family history of the condition, our Congenital Adrenal Hyperplasia Panel NGS Genetic DNA Test can provide valuable insights. Contact DNA Labs UAE today to schedule an appointment and take control of your genetic health.

 

Test NameCongenital adrenal hyperplasia Panel NGS Genetic DNA Test
Components 
Price4400.0 AED
Sample ConditionBlood or Extracted DNA or One drop Blood on FTA Card
Report Delivery3 to 4 Weeks
MethodNGS Technology
Test typeHepatology Nephrology Endocrinology Disorders
DoctorGeneral Physician
Test Department:Genetics
Pre Test InformationClinical History of Patient who is going for Congenital adrenal hyperplasia Panel NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYP11A1, CYP11B1, CYP17A1, CYP21A2, HSD3B2, POR, PRKAR1A, STAR
Test Details

Congenital adrenal hyperplasia (CAH) is a group of inherited disorders that affect the adrenal glands, which produce hormones that regulate various bodily functions. CAH can cause abnormal development of the genitals, early puberty, and other health problems.

A Congenital adrenal hyperplasia Panel NGS Genetic DNA Test is a type of genetic test that analyzes a person’s DNA to identify mutations in genes associated with CAH. The test uses next-generation sequencing (NGS) technology to read the entire genetic code of these genes, allowing for more comprehensive analysis than traditional genetic tests.

The results of the test can help diagnose CAH, determine the type and severity of the condition, and inform treatment decisions. The test may also be used to identify carriers of CAH mutations, which can be useful for family planning.

The Congenital adrenal hyperplasia Panel NGS Genetic DNA Test is typically performed on a blood or saliva sample and is ordered by a healthcare provider. Results are usually available within a few weeks.