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NR0B1 Gene Adrenal Hypoplasia Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

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The NR0B1 gene adrenal hypoplasia genetic test is a diagnostic procedure aimed at identifying mutations in the NR0B1 gene, which are linked to adrenal hypoplasia congenita (AHC), a rare condition that affects adrenal gland development. This condition can lead to a critical deficiency in the production of adrenal hormones, which are crucial for regulating metabolism, the immune system, and blood pressure. The NR0B1 gene plays a significant role in the development and function of the adrenal glands and reproductive system. Mutations in this gene can lead to various health issues, including adrenal insufficiency and hypogonadotropic hypogonadism.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific mutations in the NR0B1 gene. The results can provide valuable information for the diagnosis, management, and treatment planning of individuals with or at risk of developing AHC. Additionally, it can be crucial for family planning decisions for affected families.

The cost of the NR0B1 gene adrenal hypoplasia genetic test at DNA Labs UAE is 4400 AED. This cost reflects the specialized nature of the test, the advanced technology used in the analysis, and the professional expertise required to interpret the results accurately.

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NR0B1 Gene Adrenal Hypoplasia Genetic Test

Components: NR0B1 Gene Adrenal Hypoplasia Genetic Test

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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for NR0B1 Gene Adrenal Hypoplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Adrenal Hypoplasia.

Test Details

The NR0B1 gene is associated with a condition called adrenal hypoplasia congenita (AHC). AHC is a rare genetic disorder that affects the development of the adrenal glands, which are responsible for producing hormones such as cortisol and aldosterone. A genetic test using next-generation sequencing (NGS) can be performed to analyze the NR0B1 gene for mutations or variations that may be causing adrenal hypoplasia. NGS allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variations associated with the condition.

This genetic test can help confirm a diagnosis of adrenal hypoplasia and identify the specific genetic mutation responsible for the condition. It can also be used for carrier testing in individuals with a family history of AHC or for prenatal testing in families at risk of having a child with the disorder. Knowing the specific genetic mutation can be helpful for understanding the underlying cause of adrenal hypoplasia, predicting the severity of the condition, and guiding treatment decisions. Additionally, genetic testing can provide valuable information for genetic counseling and family planning purposes.

Test Name NR0B1 Gene Adrenal hypoplasia 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for NR0B1 Gene Adrenal hypoplasia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Adrenal hypoplasia
Test Details

The NR0B1 gene is associated with a condition called adrenal hypoplasia congenita (AHC). AHC is a rare genetic disorder that affects the development of the adrenal glands, which are responsible for producing hormones such as cortisol and aldosterone.

A genetic test using next-generation sequencing (NGS) can be performed to analyze the NR0B1 gene for mutations or variations that may be causing adrenal hypoplasia. NGS allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variations associated with the condition.

This genetic test can help confirm a diagnosis of adrenal hypoplasia and identify the specific genetic mutation responsible for the condition. It can also be used for carrier testing in individuals with a family history of AHC or for prenatal testing in families at risk of having a child with the disorder.

Knowing the specific genetic mutation can be helpful for understanding the underlying cause of adrenal hypoplasia, predicting the severity of the condition, and guiding treatment decisions. Additionally, genetic testing can provide valuable information for genetic counseling and family planning purposes.

SKU: TEST-2158 Category:

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