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DMD Gene Muscular Dystrophy Becker Type Genetic Test Cost

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

-21%

The “DMD Gene Muscular Dystrophy Becker Type Genetic Test” is a specific diagnostic tool used to identify mutations in the DMD gene, which are responsible for Becker Muscular Dystrophy (BMD). This condition is a milder form of muscular dystrophy that primarily affects males, leading to muscle weakness and degeneration over time. Unlike its more severe counterpart, Duchenne Muscular Dystrophy, individuals with Becker Muscular Dystrophy tend to experience symptoms later in childhood or in adolescence, and the progression of the disease is generally slower.

The test is conducted at DNA Labs UAE, a reputable facility known for its comprehensive genetic testing services. By analyzing a sample of the patient’s DNA, the test can detect specific mutations in the DMD gene that are indicative of Becker Muscular Dystrophy. This information is crucial for confirming the diagnosis, understanding the severity of the condition, and informing treatment and management strategies.

The cost of the DMD Gene Muscular Dystrophy Becker Type Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the value of obtaining an accurate diagnosis and the potential to tailor treatment plans specifically to the genetic makeup of the individual can be invaluable for those affected by this condition.

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DMD Gene Muscular Dystrophy Becker Type Genetic Test

Components: DMD Gene Muscular Dystrophy Becker 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 DMD Gene Muscular Dystrophy, Becker type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DMD Gene Muscular Dystrophy, Becker type.

Test Details

The DMD gene, also known as the dystrophin gene, is associated with Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD). Both DMD and BMD are inherited muscle-wasting disorders caused by mutations in the DMD gene.

Next-generation sequencing (NGS) genetic testing is a type of genetic test that can analyze multiple genes simultaneously, including the DMD gene. This test can identify various types of mutations in the DMD gene, such as deletions, duplications, point mutations, and small insertions or deletions.

NGS genetic testing for the DMD gene can be used to diagnose DMD or BMD, determine carrier status in females, and provide genetic counseling for affected individuals and their families. It can also help in prenatal diagnosis for families at risk of having a child with DMD or BMD.

NGS genetic testing for the DMD gene typically involves obtaining a blood or saliva sample from the individual being tested. The DNA in the sample is then extracted and sequenced using NGS technology. The resulting sequence data is analyzed to identify any mutations or variants in the DMD gene.

This type of genetic testing can provide valuable information for the management and treatment of individuals with DMD or BMD, as well as for family planning decisions. It is usually performed by specialized genetic testing laboratories or genetic clinics.

Test Name DMD Gene Muscular dystrophy Becker 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 DMD Gene Muscular dystrophy, Becker type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DMD Gene Muscular dystrophy, Becker type
Test Details

The DMD gene, also known as the dystrophin gene, is associated with Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD). Both DMD and BMD are inherited muscle-wasting disorders caused by mutations in the DMD gene.

Next-generation sequencing (NGS) genetic testing is a type of genetic test that can analyze multiple genes simultaneously, including the DMD gene. This test can identify various types of mutations in the DMD gene, such as deletions, duplications, point mutations, and small insertions or deletions.

NGS genetic testing for the DMD gene can be used to diagnose DMD or BMD, determine carrier status in females, and provide genetic counseling for affected individuals and their families. It can also help in prenatal diagnosis for families at risk of having a child with DMD or BMD.

NGS genetic testing for the DMD gene typically involves obtaining a blood or saliva sample from the individual being tested. The DNA in the sample is then extracted and sequenced using NGS technology. The resulting sequence data is analyzed to identify any mutations or variants in the DMD gene.

This type of genetic testing can provide valuable information for the management and treatment of individuals with DMD or BMD, as well as for family planning decisions. It is usually performed by specialized genetic testing laboratories or genetic clinics.