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GNAS Gene Pseudohypoparathyroidism type 1A Genetic Test Cost

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

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The GNAS Gene Pseudohypoparathyroidism type 1A Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to detect mutations in the GNAS gene, which are associated with Pseudohypoparathyroidism type 1A (PHP1A). PHP1A is a rare genetic disorder characterized by resistance to the parathyroid hormone (PTH), leading to low calcium levels and high phosphate levels in the blood, alongside other physical and developmental symptoms. This test plays a crucial role in the accurate diagnosis and management of the condition, enabling tailored treatment plans for affected individuals.

The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to identify any genetic mutations in the GNAS gene. With a cost of 4400 AED, the test is an important investment for individuals with a clinical suspicion or family history of PHP1A, offering them a clear understanding of their genetic status. By choosing DNA Labs UAE for this testing, patients can expect a high level of accuracy, confidentiality, and professional support throughout the testing process.

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GNAS Gene Pseudohypoparathyroidism type 1A Genetic Test

Test Name: GNAS Gene Pseudohypoparathyroidism type 1A Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Hepatology Nephrology Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for GNAS Gene Pseudohypoparathyroidism type 1A NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GNAS Gene Pseudohypoparathyroidism type 1A NGS Genetic DNA Test gene GNAS

Test Details

The GNAS gene is responsible for producing a protein called the alpha subunit of the stimulatory G protein (Gs). This protein plays a crucial role in signaling pathways that regulate hormone production and cell function. Pseudohypoparathyroidism type 1A (PHP1A) is a genetic disorder caused by mutations in the GNAS gene. This condition is characterized by resistance to the action of parathyroid hormone (PTH), which leads to low levels of calcium in the blood (hypocalcemia) and high levels of phosphate (hyperphosphatemia). Additionally, PHP1A can cause short stature, obesity, round face, and other physical features.

Next-generation sequencing (NGS) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the GNAS gene. This test can identify mutations or variations in the GNAS gene that may be responsible for PHP1A. By performing an NGS genetic test for PHP1A, healthcare professionals can accurately diagnose individuals with this condition. This information is crucial for appropriate management and treatment planning for affected individuals.

Test Name GNAS Gene Pseudohypoparathyroidism type 1A 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 GNAS Gene Pseudohypoparathyroidism type 1A NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GNAS Gene Pseudohypoparathyroidism type 1A NGS Genetic DNA Test gene GNAS
Test Details

The GNAS gene is responsible for producing a protein called the alpha subunit of the stimulatory G protein (Gs). This protein plays a crucial role in signaling pathways that regulate hormone production and cell function.

Pseudohypoparathyroidism type 1A (PHP1A) is a genetic disorder caused by mutations in the GNAS gene. This condition is characterized by resistance to the action of parathyroid hormone (PTH), which leads to low levels of calcium in the blood (hypocalcemia) and high levels of phosphate (hyperphosphatemia). Additionally, PHP1A can cause short stature, obesity, round face, and other physical features.

Next-generation sequencing (NGS) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the GNAS gene. This test can identify mutations or variations in the GNAS gene that may be responsible for PHP1A.

By performing an NGS genetic test for PHP1A, healthcare professionals can accurately diagnose individuals with this condition. This information is crucial for appropriate management and treatment planning for affected individuals.

SKU: TEST-3774 Category:

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