Short Description

NGS genetic DNA test detecets for variant and mutation detection in LMNA gene for Hutchinson-Gilford progeria

PreTest Information

Clinical History of Patient who is going for LMNA Gene Hutchinson-Gilford progeria NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LMNA Gene Hutchinson-Gilford progeria NGS Genetic DNA Test gene LMNA

Detail Description

LMNA Gene Hutchinson-Gilford Progeria NGS Genetic DNA Test Cost INR 20000: Symptoms, Diagnosis

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder that affects about 1 in 4-8 million newborns worldwide. It is a disease that causes premature aging, which leads to a shortened lifespan. The disease is caused by a mutation in the LMNA gene. This gene is responsible for producing lamin A, a protein that helps maintain the structure of the cell nucleus.

Symptoms

The symptoms of Hutchinson-Gilford Progeria Syndrome start to appear in children between the ages of 1-2 years. The symptoms include:

• Slow growth rate
• Baldness
• Prominent scalp veins
• Thin, wrinkled skin
• Loss of body fat and muscle
• Stiff joints
• High-pitched voice
• Cardiovascular disease

Diagnosis

The diagnosis of Hutchinson-Gilford Progeria Syndrome is based on the physical symptoms of the patient. A genetic test can also be done to confirm the diagnosis. The LMNA gene mutation that causes Hutchinson-Gilford Progeria Syndrome can be detected through Next Generation Sequencing (NGS) Genetic DNA Testing.

NGS Genetic DNA Test Cost INR 20000

The cost of NGS Genetic DNA Testing for Hutchinson-Gilford Progeria Syndrome in India is INR 20000. DNA Labs India offers this test with a quick turnaround time and high accuracy. The test involves the sequencing of the patient's DNA to identify the LMNA gene mutation that causes the disease.

The NGS Genetic DNA Test for Hutchinson-Gilford Progeria Syndrome is a valuable tool for early diagnosis and management of the disease. It can help patients and their families understand the disease and plan for the future.

Conclusion

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder that causes premature aging and a shortened lifespan. The disease is caused by a mutation in the LMNA gene, which can be detected through NGS Genetic DNA Testing. DNA Labs India offers this test for INR 20000 with a quick turnaround time and high accuracy. Early diagnosis and management of the disease can help patients and their families plan for the future.

For more information about NGS Genetic DNA Testing for Hutchinson-Gilford Progeria Syndrome, please contact DNA Labs India.