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Accurate Test Results for POMT2 Gene Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 NGS Genetic DNA Test
POMT2 Gene Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 NGS Genetic DNA Test Cost 20000 Rs
POMT2 Gene Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 NGS Genetic DNA Test Details
POMT2 Gene Muscular Dystrophy-Dystroglycanopathy (Congenital with Mental Retardation), Type B2 NGS Genetic DNA Test: Symptoms, Diagnosis and Cost
Muscular dystrophy is a group of inherited diseases that cause progressive muscle weakness and wasting. POMT2 gene muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 is a rare form of muscular dystrophy that affects the muscles and the brain. This type of muscular dystrophy is caused by a mutation in the POMT2 gene, which is responsible for producing a protein that helps to build the outer layer of muscle cells. When this protein is not produced correctly, it causes the muscles to weaken and waste away.
Symptoms of POMT2 Gene Muscular Dystrophy-Dystroglycanopathy (Congenital with Mental Retardation), Type B2
The symptoms of POMT2 gene muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 can vary depending on the severity of the disease. Some of the common symptoms include:
- Muscle weakness and wasting
- Delayed motor development
- Intellectual disability
- Seizures
- Speech difficulties
- Vision problems
- Difficulty swallowing
- Abnormal eye movements
Diagnosis of POMT2 Gene Muscular Dystrophy-Dystroglycanopathy (Congenital with Mental Retardation), Type B2
The diagnosis of POMT2 gene muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 is usually made through a combination of physical examination, family history, and genetic testing. A muscle biopsy may also be performed to confirm the diagnosis.
NGS Genetic DNA Test for POMT2 Gene Muscular Dystrophy-Dystroglycanopathy (Congenital with Mental Retardation), Type B2
The NGS genetic DNA test for POMT2 gene muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 is a genetic test that can detect mutations in the POMT2 gene. This test is performed using next-generation sequencing (NGS) technology, which allows for the rapid and accurate analysis of DNA sequences.
Cost of NGS Genetic DNA Test for POMT2 Gene Muscular Dystrophy-Dystroglycanopathy (Congenital with Mental Retardation), Type B2
The cost of the NGS genetic DNA test for POMT2 gene muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 is approximately INR 20,000 in India. This cost may vary depending on the specific laboratory and location.
Conclusion
POMT2 gene muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 is a rare form of muscular dystrophy that can cause muscle weakness, intellectual disability, and other symptoms. Genetic testing using NGS technology can help to diagnose this condition and provide valuable information for treatment and management. If you or someone you know is experiencing symptoms of POMT2 gene muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2, it is important to seek medical attention and consider genetic testing.
For more information on genetic testing for POMT2 gene muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2, please contact DNA Labs India.
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 POMT2 Gene Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 NGS Genetic DNA Test
