Short Description

NGS genetic DNA test detecets for variant and mutation detection in SGCD gene for Limb-girdle muscular dystrophy, autosomal recessice type 2F

PreTest Information

Clinical History of Patient who is going for SGCD Gene Limb-girdle muscular dystrophy, autosomal recessice type 2F NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SGCD Gene Limb-girdle muscular dystrophy, autosomal recessice type 2F

Detail Description

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

SGCD Gene Limb-girdle Muscular Dystrophy is an inherited neuromuscular disorder that affects the muscles in the hip and shoulder regions of the body. This condition is caused by mutations in the SGCD gene, which provides instructions for making a protein called delta-sarcoglycan. This protein is essential for the normal functioning of muscle cells. SGCD Gene Limb-girdle Muscular Dystrophy is an autosomal recessive disorder, meaning that an individual must inherit two copies of the mutated gene (one from each parent) to develop the condition.

Symptoms of SGCD Gene Limb-girdle Muscular Dystrophy

The symptoms of SGCD Gene Limb-girdle Muscular Dystrophy usually appear in childhood or adolescence, but they can also develop in adulthood. The most common symptoms of this condition include:

• Muscle weakness in the hip and shoulder regions of the body
• Difficulty climbing stairs or standing up from a seated position
• Waddling gait
• Difficulty lifting objects or raising the arms above the head
• Progressive muscle weakness and wasting
• Difficulty with breathing and swallowing in severe cases

Diagnosis of SGCD Gene Limb-girdle Muscular Dystrophy

Diagnosing SGCD Gene Limb-girdle Muscular Dystrophy usually involves a combination of clinical examination, genetic testing, and imaging studies. A doctor will perform a physical examination to assess muscle strength, reflexes, and coordination. Blood tests may also be conducted to check for elevated levels of muscle enzymes. Genetic testing is the most definitive method of diagnosing SGCD Gene Limb-girdle Muscular Dystrophy. This involves analyzing a blood or saliva sample to look for mutations in the SGCD gene. Imaging studies, such as magnetic resonance imaging (MRI), may also be used to assess muscle structure and function.

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

NGS Genetic DNA testing is a highly accurate and efficient method of diagnosing SGCD Gene Limb-girdle Muscular Dystrophy. The cost of this test may vary depending on the laboratory and location, but typically ranges from INR 15,000 to INR 20,000 in India. Some insurance plans may cover the cost of genetic testing, so it is important to check with your provider before undergoing testing.

Conclusion

SGCD Gene Limb-girdle Muscular Dystrophy is a rare neuromuscular disorder that can cause significant muscle weakness and disability. Early diagnosis is essential for managing symptoms and preventing complications. If you or a loved one are experiencing symptoms of SGCD Gene Limb-girdle Muscular Dystrophy, it is important to speak with a healthcare provider and consider genetic testing to determine the underlying cause of the condition.

Contact DNA Labs India for more information on SGCD Gene Limb-girdle Muscular Dystrophy and NGS Genetic DNA testing.

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 SGCD Gene Limb-girdle muscular dystrophy, autosomal recessice type 2F NGS Genetic DNA Test