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SGCG Gene Limb-girdle muscular dystrophy autosomal recessive type 2C Genetic Test

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

-21%

The SGCG gene plays a crucial role in the development and function of muscles in the body. Mutations in this gene can lead to a condition known as limb-girdle muscular dystrophy type 2C (LGMD2C), which is an autosomal recessive disorder. This means that an individual must inherit two copies of the mutated gene, one from each parent, to be affected by the condition. LGMD2C primarily affects the voluntary muscles around the hips and shoulders (the limb-girdle muscles), leading to progressive weakness and wasting of these muscle groups.

Genetic testing for mutations in the SGCG gene is a critical step in diagnosing LGMD2C. This test can confirm the presence of mutations in the gene, helping in the diagnosis and management of the condition. At DNA Labs UAE, individuals can undergo the SGCG gene test, which is a sophisticated genetic analysis aimed at identifying mutations associated with limb-girdle muscular dystrophy type 2C.

The cost of the SGCG gene test at DNA Labs UAE is 4400 AED. This test is conducted with high precision and accuracy, utilizing advanced genetic sequencing technologies to detect mutations in the SGCG gene. By opting for this test, patients and their families can gain valuable insights into the genetic basis of their condition, enabling them to make informed decisions about treatment and management options.

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SGCG Gene Limb-girdle muscular dystrophy autosomal recessive type 2C Genetic Test

Components: SGCG Gene Limb-girdle muscular dystrophy autosomal recessive type 2C 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 SGCG Gene Limb-girdle muscular dystrophy, autosomal recessive type 2C NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SGCG Gene Limb-girdle muscular dystrophy, autosomal recessive type 2C

Test Details: SGCG gene limb-girdle muscular dystrophy, autosomal recessive type 2C NGS genetic test is a genetic test that analyzes the SGCG gene for mutations associated with limb-girdle muscular dystrophy, autosomal recessive type 2C (LGMD2C). LGMD2C is a rare genetic disorder characterized by progressive muscle weakness and wasting primarily affecting the muscles of the shoulders, upper arms, and hips. It is caused by mutations in the SGCG gene, which provides instructions for making a protein called gamma-sarcoglycan. This protein is an essential component of a complex of proteins that helps maintain the structure and function of muscle cells. The NGS (Next-Generation Sequencing) genetic test is a high-throughput method that can rapidly sequence the entire SGCG gene and identify any mutations or genetic variants that may be present. This test can help confirm a diagnosis of LGMD2C and provide information about the specific genetic variant causing the condition. Knowing the specific genetic mutation can be important for determining the inheritance pattern of the disease, providing accurate genetic counseling, and potentially guiding treatment options in the future. It can also help in identifying at-risk family members who may carry the same mutation. It is important to note that this genetic test should be ordered and interpreted by a healthcare professional with expertise in genetics. Genetic counseling is also recommended both before and after the test to discuss the potential implications of the results.

Test Name SGCG Gene Limb-girdle muscular dystrophy autosomal recessive type 2C 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 SGCG Gene Limb-girdle muscular dystrophy, autosomal recessive type 2C NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SGCG Gene Limb-girdle muscular dystrophy, autosomal recessive type 2C
Test Details

SGCG gene limb-girdle muscular dystrophy, autosomal recessive type 2C NGS genetic test is a genetic test that analyzes the SGCG gene for mutations associated with limb-girdle muscular dystrophy, autosomal recessive type 2C (LGMD2C).

LGMD2C is a rare genetic disorder characterized by progressive muscle weakness and wasting primarily affecting the muscles of the shoulders, upper arms, and hips. It is caused by mutations in the SGCG gene, which provides instructions for making a protein called gamma-sarcoglycan. This protein is an essential component of a complex of proteins that helps maintain the structure and function of muscle cells.

The NGS (Next-Generation Sequencing) genetic test is a high-throughput method that can rapidly sequence the entire SGCG gene and identify any mutations or genetic variants that may be present. This test can help confirm a diagnosis of LGMD2C and provide information about the specific genetic variant causing the condition.

Knowing the specific genetic mutation can be important for determining the inheritance pattern of the disease, providing accurate genetic counseling, and potentially guiding treatment options in the future. It can also help in identifying at-risk family members who may carry the same mutation.

It is important to note that this genetic test should be ordered and interpreted by a healthcare professional with expertise in genetics. Genetic counseling is also recommended both before and after the test to discuss the potential implications of the results.