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TBCE Gene Hypoparathyroidism-Retardation-Dysmorphism Syndrome Genetic Test Cost

Name: TBCE Gene Hypoparathyroidism-Retardation-Dysmorphism Syndrome Genetic Test Cost
SKU: TEST-3674
Price: 4400 AED
Availability: InStock

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

-21%

The TBCE Gene Hypoparathyroidism-Retardation-Dysmorphism (HRD) Syndrome Genetic Test is a specialized diagnostic tool designed to detect mutations in the TBCE gene, which are responsible for the rare genetic disorder known as HRD syndrome. This condition is characterized by a combination of hypoparathyroidism, developmental delays, and distinctive facial and skeletal dysmorphisms. The test plays a crucial role in confirming the diagnosis, enabling early intervention and management of the syndrome.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, typically through a blood draw, from the individual suspected of having HRD syndrome. The laboratory then analyzes the TBCE gene for specific mutations that are indicative of the condition.

The cost of the TBCE Gene Hypoparathyroidism-Retardation-Dysmorphism Syndrome Genetic Test at DNA Labs UAE is set at 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify the genetic mutations associated with HRD syndrome. Patients and healthcare providers considering this test can expect a high level of accuracy and reliability from DNA Labs UAE, contributing to better-informed decisions regarding treatment and management of the syndrome.

Description

TBCE Gene Hypoparathyroidism-retardation-dysmorphism syndrome Genetic Test

Components: TBCE Gene Hypoparathyroidism-retardation-dysmorphism syndrome 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: Hepatology Nephrology Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for TBCE Gene Hypoparathyroidism-retardation-dysmorphism syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TBCE Gene Hypoparathyroidism-retardation-dysmorphism syndrome NGS Genetic DNA Test gene TBCE

Test Details: TBCE gene hypoparathyroidism-retardation-dysmorphism syndrome is a rare genetic disorder characterized by a combination of hypoparathyroidism, intellectual disability, and distinct facial features. It is caused by mutations in the TBCE gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of various genetic mutations or changes in a single test, making it a powerful tool for diagnosing genetic disorders. In the case of TBCE gene hypoparathyroidism-retardation-dysmorphism syndrome, NGS genetic testing can be used to identify mutations in the TBCE gene. This can help confirm the diagnosis of the syndrome and provide valuable information for genetic counseling and management of the condition.

Test Name	TBCE Gene Hypoparathyroidism-retardation-dysmorphism syndrome 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 TBCE Gene Hypoparathyroidism-retardation-dysmorphism syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TBCE Gene Hypoparathyroidism-retardation-dysmorphism syndrome NGS Genetic DNA Test gene TBCE
Test Details	TBCE gene hypoparathyroidism-retardation-dysmorphism syndrome is a rare genetic disorder characterized by a combination of hypoparathyroidism, intellectual disability, and distinct facial features. It is caused by mutations in the TBCE gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of various genetic mutations or changes in a single test, making it a powerful tool for diagnosing genetic disorders. In the case of TBCE gene hypoparathyroidism-retardation-dysmorphism syndrome, NGS genetic testing can be used to identify mutations in the TBCE gene. This can help confirm the diagnosis of the syndrome and provide valuable information for genetic counseling and management of the condition.