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LAMB1 Gene Lissencephaly Type 5 Genetic Test Cost

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

-21%

The LAMB1 gene plays a crucial role in brain development, and mutations in this gene are associated with Lissencephaly Type 5, a rare genetic disorder characterized by abnormal brain formation. This condition leads to significant neurological impairments, including developmental delay, intellectual disability, and seizures. Early and accurate diagnosis through genetic testing is vital for the management and treatment of the condition.

DNA Labs UAE offers a comprehensive genetic test specifically targeting the LAMB1 gene to identify mutations linked to Lissencephaly Type 5. The test is meticulously designed to provide reliable results, aiding in the early detection and enabling healthcare providers to devise appropriate intervention strategies for affected individuals.

The cost of the LAMB1 Gene Lissencephaly Type 5 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the advanced molecular techniques and expert analysis required to ensure accurate diagnosis. By choosing this test, patients and their families can gain valuable insights into the genetic underpinnings of Lissencephaly Type 5, facilitating informed decisions about care and management.

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  • This test is not intended for medical diagnosis or treatment
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LAMB1 Gene Lissencephaly type 5 Genetic Test

Cost: 4400.0 AED

Test Components

  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test type: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for LAMB1 Gene Lissencephaly type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LAMB1 Gene Lissencephaly type 5 NGS Genetic DNA Test gene LAMB1.

Test Details

The LAMB1 gene is associated with a rare genetic disorder called lissencephaly type 5. Lissencephaly is a condition characterized by the absence or underdevelopment of the folds and grooves (gyri and sulci) in the brain, leading to a smooth brain surface. This condition can cause severe intellectual disability, developmental delays, seizures, and other neurological problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously, providing a comprehensive evaluation of an individual’s genetic makeup. In the case of lissencephaly type 5, NGS genetic testing can be used to identify mutations or variations in the LAMB1 gene that are associated with the condition.

The NGS genetic test for lissencephaly type 5 typically involves collecting a DNA sample from the individual, usually through a blood sample or a cheek swab. The DNA is then sequenced using advanced technologies to identify any variations or mutations in the LAMB1 gene.

The results of the test can help in confirming a diagnosis, providing information about the specific genetic variant involved, and guiding treatment and management options for the individual. It’s important to note that genetic testing for lissencephaly type 5 and other genetic disorders should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support throughout the testing process.

Test Name LAMB1 Gene Lissencephaly type 5 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for LAMB1 Gene Lissencephaly type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LAMB1 Gene Lissencephaly type 5 NGS Genetic DNA Test gene LAMB1
Test Details

The LAMB1 gene is associated with a rare genetic disorder called lissencephaly type 5. Lissencephaly is a condition characterized by the absence or underdevelopment of the folds and grooves (gyri and sulci) in the brain, leading to a smooth brain surface. This condition can cause severe intellectual disability, developmental delays, seizures, and other neurological problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously, providing a comprehensive evaluation of an individual’s genetic makeup. In the case of lissencephaly type 5, NGS genetic testing can be used to identify mutations or variations in the LAMB1 gene that are associated with the condition.

The NGS genetic test for lissencephaly type 5 typically involves collecting a DNA sample from the individual, usually through a blood sample or a cheek swab. The DNA is then sequenced using advanced technologies to identify any variations or mutations in the LAMB1 gene. The results of the test can help in confirming a diagnosis, providing information about the specific genetic variant involved, and guiding treatment and management options for the individual.

It’s important to note that genetic testing for lissencephaly type 5 and other genetic disorders should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support throughout the testing process.