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LHX4 Gene Pituitary Hormone Deficiency Combined Type 4 Genetic Test Cost

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

-21%

The “LHX4 Gene Pituitary Hormone Deficiency Combined Type 4 Genetic Test” is a specialized diagnostic procedure available at DNA Labs UAE, aimed at identifying mutations in the LHX4 gene. These mutations are associated with Combined Pituitary Hormone Deficiency (CPHD) type 4, a rare genetic disorder that impairs the pituitary gland’s ability to produce multiple essential hormones. This deficiency can lead to a variety of health issues, including growth hormone deficiency, thyroid-stimulating hormone deficiency, and sometimes, adrenal insufficiency, among others.

The test is crucial for early diagnosis and management of the condition, allowing for appropriate hormonal replacement therapies and interventions to mitigate the symptoms and improve the quality of life for affected individuals. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific genetic mutations in the LHX4 gene.

At DNA Labs UAE, the cost for this comprehensive genetic test is set at 4400 AED. The investment in this test is vital for families with a history of pituitary disorders, offering them a chance for early intervention and better management of the condition.

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LHX4 Gene Pituitary Hormone Deficiency Combined Type 4 Genetic Test

Test Name: LHX4 Gene Pituitary Hormone Deficiency Combined Type 4 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: Hepatology Nephrology Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for LHX4 Gene Pituitary Hormone Deficiency, Combined Type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LHX4 Gene Pituitary Hormone Deficiency, Combined Type 4 NGS Genetic DNA Test gene LHX4

Test Details

LHX4 gene pituitary hormone deficiency, combined type 4 is a rare genetic disorder that affects the production and regulation of various hormones in the pituitary gland. This condition is caused by mutations in the LHX4 gene, which is involved in the development and function of the pituitary gland.

Individuals with LHX4 gene pituitary hormone deficiency, combined type 4 may experience a range of symptoms depending on the specific hormones affected. Common symptoms may include growth hormone deficiency, hypothyroidism, adrenal insufficiency, delayed puberty, and infertility.

To diagnose LHX4 gene pituitary hormone deficiency, combined type 4, a genetic test called Next-Generation Sequencing (NGS) can be performed. NGS is a high-throughput sequencing technology that can analyze multiple genes simultaneously, providing a comprehensive assessment of genetic variations.

NGS genetic testing involves collecting a DNA sample, typically through a blood or saliva sample, and analyzing it for mutations or variations in the LHX4 gene. This test can help confirm the diagnosis of LHX4 gene pituitary hormone deficiency, combined type 4 and identify specific genetic variations that may be contributing to the condition.

Genetic testing can be beneficial for individuals with suspected LHX4 gene pituitary hormone deficiency, combined type 4, as it can provide valuable information for diagnosis, prognosis, and treatment planning. It can also help identify other family members who may be at risk of inheriting the condition.

It is important to consult with a healthcare professional or a genetic counselor to discuss the benefits, limitations, and potential implications of genetic testing before undergoing the test. They can provide guidance and support throughout the testing process and help interpret the results.

Test Name LHX4 Gene Pituitary hormone deficiency combined type 4 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for LHX4 Gene Pituitary hormone deficiency, combined type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LHX4 Gene Pituitary hormone deficiency, combined type 4 NGS Genetic DNA Test gene LHX4
Test Details

LHX4 gene pituitary hormone deficiency, combined type 4 is a rare genetic disorder that affects the production and regulation of various hormones in the pituitary gland. This condition is caused by mutations in the LHX4 gene, which is involved in the development and function of the pituitary gland.

Individuals with LHX4 gene pituitary hormone deficiency, combined type 4 may experience a range of symptoms depending on the specific hormones affected. Common symptoms may include growth hormone deficiency, hypothyroidism, adrenal insufficiency, delayed puberty, and infertility.

To diagnose LHX4 gene pituitary hormone deficiency, combined type 4, a genetic test called Next-Generation Sequencing (NGS) can be performed. NGS is a high-throughput sequencing technology that can analyze multiple genes simultaneously, providing a comprehensive assessment of genetic variations.

NGS genetic testing involves collecting a DNA sample, typically through a blood or saliva sample, and analyzing it for mutations or variations in the LHX4 gene. This test can help confirm the diagnosis of LHX4 gene pituitary hormone deficiency, combined type 4 and identify specific genetic variations that may be contributing to the condition.

Genetic testing can be beneficial for individuals with suspected LHX4 gene pituitary hormone deficiency, combined type 4, as it can provide valuable information for diagnosis, prognosis, and treatment planning. It can also help identify other family members who may be at risk of inheriting the condition.

It is important to consult with a healthcare professional or a genetic counselor to discuss the benefits, limitations, and potential implications of genetic testing before undergoing the test. They can provide guidance and support throughout the testing process and help interpret the results.

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