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TMEM127 Gene Pheochromocytoma Type 8 Genetic Test Cost

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

-21%

The TMEM127 Gene Pheochromocytoma Type 8 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the TMEM127 gene, which are linked to the development of Pheochromocytoma Type 8. Pheochromocytomas are rare, usually benign tumors that arise from the adrenal glands and can lead to excessive production of adrenaline, causing high blood pressure, heart palpitations, and other symptoms. The identification of a mutation in the TMEM127 gene can provide crucial information for individuals with a family history of the condition or those presenting symptoms suggestive of pheochromocytoma, facilitating early diagnosis and management. This genetic test is priced at 4400 AED and is conducted with state-of-the-art technology to ensure accurate and reliable results, aiding in the personalized treatment planning and genetic counseling for affected individuals and their families.

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TMEM127 Gene Pheochromocytoma type 8 Genetic Test

Test Name: TMEM127 Gene Pheochromocytoma type 8 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: Cancer

Doctor: Oncologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for TMEM127 Gene Pheochromocytoma type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TMEM127 Gene Pheochromocytoma type 8 NGS Genetic DNA Test gene TMEM127

Test Details

The TMEM127 gene is associated with Pheochromocytoma type 8, a rare genetic disorder characterized by the development of tumors in the adrenal glands called pheochromocytomas. These tumors produce excess adrenaline and noradrenaline hormones, leading to symptoms such as high blood pressure, rapid heartbeat, sweating, and anxiety.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes and identify any genetic variations or mutations. In the case of Pheochromocytoma type 8, NGS genetic testing can be performed to detect any mutations or alterations in the TMEM127 gene that may be causing the condition.

By identifying the specific genetic mutation in the TMEM127 gene, NGS testing can help confirm a diagnosis of Pheochromocytoma type 8 and provide important information for medical management and genetic counseling. It can also help identify individuals at risk of developing the condition, allowing for early detection and intervention.

Test Name TMEM127 Gene Pheochromocytoma type 8 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 Cancer
Doctor Oncologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TMEM127 Gene Pheochromocytoma type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TMEM127 Gene Pheochromocytoma type 8 NGS Genetic DNA Test gene TMEM127
Test Details

The TMEM127 gene is associated with Pheochromocytoma type 8, a rare genetic disorder characterized by the development of tumors in the adrenal glands called pheochromocytomas. These tumors produce excess adrenaline and noradrenaline hormones, leading to symptoms such as high blood pressure, rapid heartbeat, sweating, and anxiety.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes and identify any genetic variations or mutations. In the case of Pheochromocytoma type 8, NGS genetic testing can be performed to detect any mutations or alterations in the TMEM127 gene that may be causing the condition.

By identifying the specific genetic mutation in the TMEM127 gene, NGS testing can help confirm a diagnosis of Pheochromocytoma type 8 and provide important information for medical management and genetic counseling. It can also help identify individuals at risk of developing the condition, allowing for early detection and intervention.