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MED12 Gene FG Syndrome Type 1 Genetic Test

Name: MED12 Gene FG Syndrome Type 1 Genetic Test
SKU: TEST-1374
Price: 4400 AED
Availability: InStock

4,400 د.إ

-21%

The MED12 gene FG Syndrome Type 1 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, aimed at identifying mutations in the MED12 gene, which are associated with FG Syndrome Type 1. FG Syndrome is a rare genetic disorder that primarily affects males, leading to various developmental delays, intellectual disability, and physical anomalies. The test involves analyzing the patient’s DNA to detect specific alterations in the MED12 gene that are indicative of this condition.

Priced at 4400 AED, the test is conducted under the guidance of genetic experts at DNA Labs UAE, employing state-of-the-art technology to ensure accurate and reliable results. This genetic test is crucial for early diagnosis, which can significantly aid in managing the symptoms of FG Syndrome Type 1 through tailored therapeutic strategies and interventions, enhancing the quality of life for affected individuals and their families.

Description

MED12 Gene FG syndrome type 1 Genetic Test

Test Name: MED12 Gene FG syndrome type 1 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for MED12 Gene FG syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MED12 Gene FG syndrome type 1.

Test Details:

MED12 gene FG syndrome type 1 NGS genetic test is a diagnostic test that uses next-generation sequencing (NGS) technology to detect mutations in the MED12 gene associated with FG syndrome type 1. FG syndrome type 1 is a rare genetic disorder characterized by intellectual disability, facial abnormalities, and other physical and developmental abnormalities. The MED12 gene provides instructions for making a protein that is involved in regulating gene expression and is important for normal development. Mutations in this gene can disrupt normal gene expression, leading to the symptoms of FG syndrome type 1. The NGS genetic test for MED12 gene mutations can help confirm a diagnosis of FG syndrome type 1 and provide information for genetic counseling and management of the condition.

Test Name	MED12 Gene FG syndrome type 1 Genetic Test
Components
Price	4400.0 AED
Sample Condition	Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery	3 to 4 Weeks
Method	NGS Technology
Test type	Neurological Disorders
Doctor	Neurologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for MED12 Gene FG syndrome type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MED12 Gene FG syndrome type 1
Test Details	MED12 gene FG syndrome type 1 NGS genetic test is a diagnostic test that uses next-generation sequencing (NGS) technology to detect mutations in the MED12 gene associated with FG syndrome type 1. FG syndrome type 1 is a rare genetic disorder characterized by intellectual disability, facial abnormalities, and other physical and developmental abnormalities. The MED12 gene provides instructions for making a protein that is involved in regulating gene expression and is important for normal development. Mutations in this gene can disrupt normal gene expression, leading to the symptoms of FG syndrome type 1. The NGS genetic test for MED12 gene mutations can help confirm a diagnosis of FG syndrome type 1 and provide information for genetic counseling and management of the condition.