Short Description

NGS genetic DNA test detecets for variant and mutation detection in SGCG gene for Limb-girdle muscular dystrophy, autosomal recessive type 2C

PreTest 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

Detail Description

SGCG Gene Limb-girdle Muscular Dystrophy: Symptoms, Diagnosis and NGS Genetic DNA Test Cost

SGCG Gene Limb-girdle Muscular Dystrophy, Autosomal Recessive Type 2C is a rare genetic disorder that affects the muscles of the limbs and the trunk. It is caused by mutations in the SGCG gene, which provides instructions for making a protein called sarcoglycan gamma. This protein is essential for the proper function of the muscles.

Symptoms of SGCG Gene Limb-girdle Muscular Dystrophy

The symptoms of SGCG Gene Limb-girdle Muscular Dystrophy may vary from person to person. Some common symptoms include:

• Muscle weakness in the hips, thighs, and shoulders
• Difficulty walking and running
• Frequent falls
• Waddling gait
• Lordosis (an abnormal curvature of the lower spine)
• Reduced mobility of the arms and legs
• Progressive muscle wasting
• Difficulty breathing and swallowing (in severe cases)

Diagnosis of SGCG Gene Limb-girdle Muscular Dystrophy

SGCG Gene Limb-girdle Muscular Dystrophy can be diagnosed through a combination of clinical evaluation, imaging studies, and genetic testing. A doctor may perform a physical exam to assess muscle strength and mobility. They may also order imaging studies such as an MRI or CT scan to look for muscle abnormalities. Genetic testing, such as Next Generation Sequencing (NGS), can identify mutations in the SGCG gene that are responsible for the disorder.

NGS Genetic DNA Test Cost for SGCG Gene Limb-girdle Muscular Dystrophy

The cost of NGS Genetic DNA testing for SGCG Gene Limb-girdle Muscular Dystrophy in India is approximately INR 20,000. This test involves sequencing the entire SGCG gene to identify any mutations that may be responsible for the disorder. The results of this test can provide valuable information about the cause of the disease, which can help guide treatment and management options.

Conclusion

SGCG Gene Limb-girdle Muscular Dystrophy is a rare genetic disorder that can cause significant muscle weakness and mobility issues. Early diagnosis through a combination of clinical evaluation, imaging studies, and genetic testing is crucial for effective management of the disorder. NGS Genetic DNA testing can identify mutations in the SGCG gene that are responsible for the disorder, providing valuable information for treatment and management options. If you suspect that you or a loved one may be affected by this disorder, it is important to consult with a qualified healthcare provider as soon as possible.

At DNA Labs India, we offer NGS Genetic DNA testing for SGCG Gene Limb-girdle Muscular Dystrophy and other genetic disorders. Contact us today to learn more about our testing services.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for SGCG Gene Limb-girdle muscular dystrophy, autosomal recessive type 2C NGS Genetic DNA Test