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NSDHL Gene CK Syndrome Genetic Test Cost

Name: NSDHL Gene CK Syndrome Genetic Test Cost
SKU: TEST-1163
Price: 4400 AED
Availability: InStock

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

-21%

The NSDHL gene CK Syndrome Genetic Test is a specialized diagnostic tool offered at DNA Labs UAE, designed to detect mutations in the NSDHL gene, which are associated with CK Syndrome. CK Syndrome is a rare X-linked recessive genetic disorder that affects multiple systems in the body, leading to symptoms such as intellectual disability, microcephaly, facial dysmorphism, and other clinical manifestations. The test is particularly important for families with a history of the disorder, or for individuals showing symptoms, as it helps in confirming the diagnosis, understanding the risk of passing the mutation to offspring, and guiding management and treatment options. The cost of the NSDHL gene CK Syndrome Genetic Test at DNA Labs UAE is 4400 AED, making it accessible for those in need of this crucial diagnostic service.

Description

NSDHL Gene CK Syndrome Genetic Test

Components: NSDHL Gene CK 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 NSDHL Gene CK Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NSDHL Gene CK Syndrome.

Test Details:

The NSDHL gene is a gene that provides instructions for making an enzyme called 3-beta-hydroxysteroid delta-7-reductase. This enzyme is involved in the production of cholesterol and other lipids in the body. Mutations in the NSDHL gene can cause a rare genetic disorder called CK syndrome, which affects multiple organs and systems in the body.

NGS (next-generation sequencing) genetic testing is a type of genetic testing that uses advanced technology to rapidly sequence large amounts of DNA. This type of testing can be used to identify mutations in genes like NSDHL that may be responsible for genetic disorders like CK syndrome. NGS testing can be used to analyze multiple genes simultaneously, which can help to diagnose genetic disorders more quickly and accurately than traditional genetic testing methods.

Test Name	NSDHL Gene CK 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 NSDHL Gene CK syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NSDHL Gene CK syndrome
Test Details	The NSDHL gene is a gene that provides instructions for making an enzyme called 3-beta-hydroxysteroid delta-7-reductase. This enzyme is involved in the production of cholesterol and other lipids in the body. Mutations in the NSDHL gene can cause a rare genetic disorder called CK syndrome, which affects multiple organs and systems in the body. NGS (next-generation sequencing) genetic testing is a type of genetic testing that uses advanced technology to rapidly sequence large amounts of DNA. This type of testing can be used to identify mutations in genes like NSDHL that may be responsible for genetic disorders like CK syndrome. NGS testing can be used to analyze multiple genes simultaneously, which can help to diagnose genetic disorders more quickly and accurately than traditional genetic testing methods.