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NDUFAF1 Gene Leigh syndrome Genetic Test Cost

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

-21%

The NDUFAF1 Gene Leigh Syndrome Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the NDUFAF1 gene, which are associated with Leigh syndrome, a severe neurological disorder. This genetic test is critical for early detection and management of the syndrome, offering insights into the genetic makeup of the individual and enabling healthcare professionals to devise tailored treatment plans. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test ensures accuracy and reliability in results. The cost of the test is 4400 AED, reflecting the advanced technology and expertise involved in diagnosing this complex condition. Through this test, families affected by Leigh syndrome can gain a better understanding of their genetic predisposition and explore potential therapeutic interventions.

Description

NDUFAF1 Gene Leigh Syndrome Genetic Test

Components: NDUFAF1 Gene Leigh 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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for NDUFAF1 Gene Leigh syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF1 Gene Leigh syndrome.

Test Details:

The NDUFAF1 gene is associated with Leigh syndrome, a rare and severe neurological disorder. Leigh syndrome is characterized by progressive loss of mental and movement abilities, as well as other symptoms such as muscle weakness, difficulty swallowing, and respiratory problems.

Next-generation sequencing (NGS) is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the NDUFAF1 gene. NGS can detect mutations or variations in the gene that may be responsible for Leigh syndrome.

A genetic test for Leigh syndrome using NGS involves sequencing the DNA of an individual to identify any changes or mutations in the NDUFAF1 gene. This can help in diagnosing Leigh syndrome and determining the underlying genetic cause of the disorder.

It is important to note that genetic testing for Leigh syndrome should be conducted by a qualified healthcare professional or genetic counselor, who can provide appropriate counseling and interpretation of the results. Genetic testing may also involve testing other genes associated with Leigh syndrome, as there are several genes that can contribute to the disorder.

Test Name	NDUFAF1 Gene Leigh syndrome 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 NDUFAF1 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF1 Gene Leigh syndrome
Test Details	The NDUFAF1 gene is associated with Leigh syndrome, a rare and severe neurological disorder. Leigh syndrome is characterized by progressive loss of mental and movement abilities, as well as other symptoms such as muscle weakness, difficulty swallowing, and respiratory problems. Next-generation sequencing (NGS) is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the NDUFAF1 gene. NGS can detect mutations or variations in the gene that may be responsible for Leigh syndrome. A genetic test for Leigh syndrome using NGS involves sequencing the DNA of an individual to identify any changes or mutations in the NDUFAF1 gene. This can help in diagnosing Leigh syndrome and determining the underlying genetic cause of the disorder. It is important to note that genetic testing for Leigh syndrome should be conducted by a qualified healthcare professional or genetic counselor, who can provide appropriate counseling and interpretation of the results. Genetic testing may also involve testing other genes associated with Leigh syndrome, as there are several genes that can contribute to the disorder.