Sale!

TSHR Gene Hypothyroidism Congenital Nongoitrous Type 1 Genetic Test

Name: TSHR Gene Hypothyroidism Congenital Nongoitrous Type 1 Genetic Test
SKU: TEST-3676
Price: 4400 AED
Availability: InStock

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

-21%

The “TSHR Gene Hypothyroidism Congenital Nongoitrous Type 1 Genetic Test” is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the TSHR gene, which are responsible for Congenital Nongoitrous Hypothyroidism Type 1. This condition is a form of thyroid dysgenesis where the thyroid gland is present but functions improperly or not at all, leading to decreased levels of thyroid hormone from birth. It is a critical test for early detection and management of this condition, which, if untreated, can lead to growth failure, intellectual disability, and other health issues.

The test involves collecting a DNA sample, usually through a blood draw, and analyzing the TSHR gene for specific mutations. The TSHR (Thyroid Stimulating Hormone Receptor) gene plays a pivotal role in the regulation of thyroid gland development and function. Mutations in this gene can lead to impaired thyroid hormone production, necessitating lifelong thyroid hormone replacement therapy for affected individuals.

DNA Labs UAE offers this test for a cost of 4400 AED. The price reflects the comprehensive analysis and the specialized technology required to accurately identify mutations in the TSHR gene. For families with a history of thyroid disorders or newborns showing symptoms suggestive of hypothyroidism, this test provides essential information for early intervention and treatment planning, aiming to mitigate the potential impacts of the condition on growth and development.

Description

TSHR Gene Hypothyroidism congenital nongoitrous type 1 Genetic Test

Test Name: TSHR Gene Hypothyroidism congenital nongoitrous type 1 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 TSHR Gene Hypothyroidism congenital nongoitrous type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TSHR Gene Hypothyroidism congenital nongoitrous type 1 NGS Genetic DNA Test gene TSHR

Test Details: The TSHR gene is associated with a condition called congenital nongoitrous hypothyroidism type 1. This genetic disorder is characterized by an underactive thyroid gland from birth, leading to reduced production of thyroid hormones. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes, including the TSHR gene. It allows for the detection of genetic variations or mutations that may be responsible for the development of certain diseases or conditions, such as congenital nongoitrous hypothyroidism type 1. By performing an NGS genetic test on the TSHR gene, healthcare professionals can identify specific mutations or variations that may be causing the hypothyroidism. This information can help in diagnosing the condition, determining the mode of inheritance, and providing appropriate treatment or management strategies. It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide accurate and comprehensive information about the implications of the test results.

Test Name	TSHR Gene Hypothyroidism congenital nongoitrous type 1 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 TSHR Gene Hypothyroidism congenital nongoitrous type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TSHR Gene Hypothyroidism congenital nongoitrous type 1 NGS Genetic DNA Test gene TSHR
Test Details	The TSHR gene is associated with a condition called congenital nongoitrous hypothyroidism type 1. This genetic disorder is characterized by an underactive thyroid gland from birth, leading to reduced production of thyroid hormones. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes, including the TSHR gene. It allows for the detection of genetic variations or mutations that may be responsible for the development of certain diseases or conditions, such as congenital nongoitrous hypothyroidism type 1. By performing an NGS genetic test on the TSHR gene, healthcare professionals can identify specific mutations or variations that may be causing the hypothyroidism. This information can help in diagnosing the condition, determining the mode of inheritance, and providing appropriate treatment or management strategies. It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide accurate and comprehensive information about the implications of the test results.