Short Description

NGS genetic DNA test detecets for variant and mutation detection in LMNB1 gene for Leukodystrophy demyelinating adult-onset, autosomal dominant

PreTest Information

Clinical History of Patient who is going for LMNB1 Gene Leukodystrophy demyelinating adult-onset, autosomal dominant NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with LMNB1 Gene Leukodystrophy demyelinating adult-onset, autosomal dominant

Detail Description

LMNB1 Gene Leukodystrophy Demyelinating Adult-Onset: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

Leukodystrophies are a group of rare genetic disorders that affect the white matter of the brain. These disorders are characterized by the abnormal growth or maintenance of the myelin sheath, which is the protective covering that surrounds nerve fibers. One such leukodystrophy is caused by mutations in the LMNB1 gene, which leads to demyelinating adult-onset leukodystrophy. In this blog, we will discuss the symptoms, diagnosis, and NGS genetic DNA test cost for LMNB1 gene leukodystrophy.

Symptoms of LMNB1 Gene Leukodystrophy

LMNB1 gene leukodystrophy is a rare condition that usually affects adults. The symptoms of this condition vary depending on the severity of the disease and the age of onset. Some common symptoms of this condition include:

• Weakness in the limbs
• Difficulty walking or standing
• Tremors
• Loss of sensation in the limbs
• Bladder and bowel dysfunction
• Cognitive impairment
• Depression and anxiety

The symptoms of LMNB1 gene leukodystrophy usually progress slowly over time and can lead to severe disability.

Diagnosis of LMNB1 Gene Leukodystrophy

Diagnosing LMNB1 gene leukodystrophy can be challenging because the symptoms can be similar to other neurological disorders. A comprehensive neurological exam, imaging tests, and genetic testing can help diagnose this condition. MRI scans can reveal abnormalities in the white matter of the brain, and genetic testing can identify mutations in the LMNB1 gene.

NGS Genetic DNA Test Cost for LMNB1 Gene Leukodystrophy

NGS genetic DNA testing is a powerful tool for diagnosing genetic disorders such as LMNB1 gene leukodystrophy. This test can identify mutations in the LMNB1 gene with high accuracy and can help with early diagnosis and treatment of the disease. The cost of NGS genetic DNA testing for LMNB1 gene leukodystrophy in India is around INR 20,000.

Conclusion

LMNB1 gene leukodystrophy is a rare genetic disorder that affects the white matter of the brain. The symptoms of this condition can be challenging to diagnose, but NGS genetic DNA testing can help with early diagnosis and treatment. If you or a loved one is experiencing symptoms of LMNB1 gene leukodystrophy, it is essential to seek medical attention promptly.

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 LMNB1 Gene Leukodystrophy demyelinating adult-onset, autosomal dominant NGS Genetic DNA Test