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DES Gene Neurogenic Scapuloperoneal Syndrome Kaeser Type Genetic Test Cost

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

-21%

The DES Gene Neurogenic Scapuloperoneal Syndrome Kaeser Type Genetic Test is a specialized diagnostic assessment available at DNA Labs UAE, designed to identify mutations in the DES gene, which are associated with Neurogenic Scapuloperoneal Syndrome Kaeser Type (NSPKT). This condition is a rare genetic disorder characterized by muscle weakness and atrophy, primarily affecting the shoulder girdle and lower legs. It can also involve cardiac and respiratory muscles in some cases, making early detection and management crucial.

The test involves analyzing the patient’s DNA to look for specific genetic alterations in the DES gene that are known to cause NSPKT. This is vital for confirming the diagnosis, understanding the disease’s progression, and guiding treatment strategies. It also provides essential information for family planning and genetic counseling for affected families.

The cost of the DES Gene Neurogenic Scapuloperoneal Syndrome Kaeser Type Genetic Test at DNA Labs UAE is 4400 AED. The testing process is conducted with the highest standards of accuracy and confidentiality, ensuring patients receive comprehensive support throughout the diagnostic journey. Given the complexity and rarity of the condition, having access to such a targeted genetic test represents a significant step forward in personalized medicine and the management of genetic disorders.

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DES Gene Neurogenic scapuloperoneal syndrome Kaeser type 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 DES Gene Neurogenic scapuloperoneal syndrome, Kaeser type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DES Gene Neurogenic scapuloperoneal syndrome, Kaeser type.

Test Details

The DES gene, also known as desmin, is associated with a condition called neurogenic scapuloperoneal syndrome, Kaeser type. This genetic disorder affects the muscles and nerves in the shoulders and lower legs. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of neurogenic scapuloperoneal syndrome, Kaeser type, NGS genetic testing can be used to identify any mutations or variations in the DES gene that may be causing the condition. By analyzing the DES gene, NGS genetic testing can provide valuable information about the specific genetic changes that are present in an individual. This information can help with diagnosis, prognosis, and treatment decisions for individuals with neurogenic scapuloperoneal syndrome, Kaeser type.

Test Name DES Gene Neurogenic scapuloperoneal syndrome Kaeser type 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 DES Gene Neurogenic scapuloperoneal syndrome, Kaeser type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DES Gene Neurogenic scapuloperoneal syndrome, Kaeser type
Test Details

The DES gene, also known as desmin, is associated with a condition called neurogenic scapuloperoneal syndrome, Kaeser type. This genetic disorder affects the muscles and nerves in the shoulders and lower legs.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of neurogenic scapuloperoneal syndrome, Kaeser type, NGS genetic testing can be used to identify any mutations or variations in the DES gene that may be causing the condition.

By analyzing the DES gene, NGS genetic testing can provide valuable information about the specific genetic changes that are present in an individual. This information can help with diagnosis, prognosis, and treatment decisions for individuals with neurogenic scapuloperoneal syndrome, Kaeser type.