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LMNB1 Gene Leukodystrophy demyelinating adult-onset autosomal dominant Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The LMNB1 gene leukodystrophy, also known as adult-onset autosomal dominant demyelinating leukodystrophy, is a rare genetic disorder characterized by progressive damage to the myelin sheath, the protective covering of the nerves in the central nervous system. This condition leads to a range of neurological symptoms, including walking difficulties, muscle stiffness, and in some cases, cognitive decline. The disorder is caused by mutations in the LMNB1 gene, which plays a crucial role in the structure and function of the nuclear envelope.

To diagnose this condition, genetic testing is available at DNA Labs UAE. The test specifically looks for mutations in the LMNB1 gene that are known to cause the disorder. It is a crucial step for affected individuals and their families, as it can confirm the diagnosis, inform about the progression of the disease, and guide treatment and management options. The test is also vital for understanding the risk of passing the condition to future generations, as it follows an autosomal dominant inheritance pattern, meaning only one copy of the altered gene is sufficient to cause the disorder.

The cost of the LMNB1 gene leukodystrophy genetic test at DNA Labs UAE is 4400 AED. This investment can provide essential information for the accurate diagnosis and personalized management of the condition, offering affected individuals and their families a clearer understanding of the disorder and how to best tackle its challenges.

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LMNB1 Gene Leukodystrophy Demyelinating Adult-Onset Autosomal Dominant Genetic Test

Test Name: LMNB1 Gene Leukodystrophy Demyelinating Adult-Onset Autosomal Dominant Genetic Test

  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics
  • Pre Test 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.

Test Details

The LMNB1 gene is associated with a type of leukodystrophy called adult-onset demyelinating leukodystrophy. Leukodystrophies are a group of genetic disorders that affect the white matter of the brain, leading to a loss of myelin, the protective covering of nerve fibers. In the case of LMNB1-related leukodystrophy, the condition typically manifests in adulthood, usually between the ages of 20 and 50. It is inherited in an autosomal dominant manner, meaning that an affected individual has a 50% chance of passing on the gene mutation to each of their children.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, allowing for a more comprehensive evaluation of genetic variations. In the context of LMNB1-related leukodystrophy, NGS genetic testing can identify specific mutations or variations in the LMNB1 gene that may be responsible for the condition. By undergoing NGS genetic testing for LMNB1-related leukodystrophy, individuals and their families can gain a better understanding of the genetic basis of the condition, which can inform medical management and genetic counseling decisions.

Test Name LMNB1 Gene Leukodystrophy demyelinating adult-onset autosomal dominant Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test 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
Test Details

The LMNB1 gene is associated with a type of leukodystrophy called adult-onset demyelinating leukodystrophy. Leukodystrophies are a group of genetic disorders that affect the white matter of the brain, leading to a loss of myelin, the protective covering of nerve fibers.

In the case of LMNB1-related leukodystrophy, the condition typically manifests in adulthood, usually between the ages of 20 and 50. It is inherited in an autosomal dominant manner, meaning that an affected individual has a 50% chance of passing on the gene mutation to each of their children.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, allowing for a more comprehensive evaluation of genetic variations. In the context of LMNB1-related leukodystrophy, NGS genetic testing can identify specific mutations or variations in the LMNB1 gene that may be responsible for the condition.

By undergoing NGS genetic testing for LMNB1-related leukodystrophy, individuals and their families can gain a better understanding of the genetic basis of the condition, which can inform medical management and genetic counseling decisions.