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FERMT3 Gene Leukocyte Adhesion Deficiency Type 3 Genetic Test Cost

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

-21%

The FERMT3 Gene Leukocyte Adhesion Deficiency Type 3 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the FERMT3 gene that are responsible for Leukocyte Adhesion Deficiency Type 3 (LAD3). This condition is a rare, autosomal recessive immune disorder characterized by the body’s inability to properly control infection, leading to severe, recurrent infections and delayed wound healing. The test is crucial for early diagnosis and management of the condition, enabling targeted treatments and interventions that can significantly improve the quality of life for affected individuals. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately analyze and interpret the genetic data. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test represents a vital resource for families at risk of LAD3, providing them with essential information for making informed health decisions.

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FERMT3 Gene Leukocyte adhesion deficiency type 3 Genetic Test

Test Name: FERMT3 Gene Leukocyte adhesion deficiency type 3 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Hematology

Doctor: Hematologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for FERMT3 Gene Leukocyte adhesion deficiency type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FERMT3 Gene Leukocyte adhesion deficiency type 3 NGS Genetic DNA Test gene FERMT3

Test Details

The FERMT3 gene is associated with a condition called leukocyte adhesion deficiency type 3 (LAD3). LAD3 is a rare genetic disorder that affects the immune system. It is characterized by impaired adhesion and migration of white blood cells, which leads to recurrent infections, delayed wound healing, and other immune-related problems.

NGS (Next-Generation Sequencing) genetic testing refers to a method used to analyze and sequence a person’s DNA. It allows for the simultaneous analysis of multiple genes, including the FERMT3 gene, to identify any genetic variations or mutations that may be associated with LAD3. This type of testing can help diagnose individuals with suspected LAD3 and provide information about their genetic risk for the condition.

NGS genetic testing for FERMT3 gene mutations can be helpful in confirming a diagnosis of LAD3 and guiding treatment decisions. It can also be used for carrier testing in families with a history of LAD3, allowing individuals to determine their risk of passing the condition on to their children.

It is important to note that genetic testing should be conducted under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.

Test Name FERMT3 Gene Leukocyte adhesion deficiency type 3 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 Hematology
Doctor Hematologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FERMT3 Gene Leukocyte adhesion deficiency type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FERMT3 Gene Leukocyte adhesion deficiency type 3 NGS Genetic DNA Test gene FERMT3
Test Details

The FERMT3 gene is associated with a condition called leukocyte adhesion deficiency type 3 (LAD3). LAD3 is a rare genetic disorder that affects the immune system. It is characterized by impaired adhesion and migration of white blood cells, which leads to recurrent infections, delayed wound healing, and other immune-related problems.

NGS (Next-Generation Sequencing) genetic testing refers to a method used to analyze and sequence a person’s DNA. It allows for the simultaneous analysis of multiple genes, including the FERMT3 gene, to identify any genetic variations or mutations that may be associated with LAD3. This type of testing can help diagnose individuals with suspected LAD3 and provide information about their genetic risk for the condition.

NGS genetic testing for FERMT3 gene mutations can be helpful in confirming a diagnosis of LAD3 and guiding treatment decisions. It can also be used for carrier testing in families with a history of LAD3, allowing individuals to determine their risk of passing the condition on to their children.

It is important to note that genetic testing should be conducted under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.