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ITGA7 Gene Myopathy Due to Integrin 7A Deficiency Genetic Test Cost

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

-21%

The “ITGA7 Gene Myopathy Due to Integrin 7A Deficiency Genetic Test” is a specialized diagnostic examination aimed at identifying mutations in the ITGA7 gene, which can lead to a rare form of myopathy. Myopathy associated with ITGA7 gene mutations is characterized by muscle weakness and reduced muscle mass due to a deficiency in integrin alpha-7, a protein essential for muscle cell structure and function. This condition is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected by the disorder.

The test is performed at DNA Labs UAE, a leading facility in genetic diagnostics and research. The procedure involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed for specific mutations in the ITGA7 gene that are known to cause the condition. This genetic test is crucial for accurate diagnosis, allowing for appropriate management and treatment plans to be developed for affected individuals.

The cost of the ITGA7 Gene Myopathy Due to Integrin 7A Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This cost covers the genetic analysis and a comprehensive report that details the findings. For patients suspected of having this rare form of myopathy, or for those with a family history of the condition, this test provides a valuable tool for confirming the diagnosis and facilitating early intervention strategies.

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ITGA7 Gene Myopathy due to Integrin 7A deficiency Genetic Test

Components: ITGA7 Gene Myopathy due to Integrin 7A deficiency Genetic Test

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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for ITGA7 Gene Myopathy due to Integrin 7A deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ITGA7 Gene Myopathy due to Integrin 7A deficiency.

Test Details: ITGA7 gene myopathy is a rare genetic disorder caused by mutations in the ITGA7 gene. This gene provides instructions for making a protein called integrin alpha-7 (7). Integrins are a group of proteins that are involved in cell adhesion and signaling processes. Integrin alpha-7 is mainly found in skeletal and cardiac muscle cells, where it plays a crucial role in maintaining the structural integrity and function of these muscles. Mutations in the ITGA7 gene can lead to a deficiency or dysfunction of integrin alpha-7, resulting in muscle weakness and wasting. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the identification of mutations or variations in the DNA sequence of specific genes, including the ITGA7 gene. NGS genetic testing for ITGA7 gene myopathy can help confirm a diagnosis and identify the specific genetic mutation causing the condition. This information can be important for understanding the underlying cause of the disease, predicting disease progression, and guiding treatment decisions. If you suspect that you or someone you know may have ITGA7 gene myopathy, it is recommended to consult with a healthcare professional or a genetic counselor who can provide more information about the testing process and help interpret the results.

Test Name ITGA7 Gene Myopathy due to Integrin 7A deficiency 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 ITGA7 Gene Myopathy due to Integrin 7A deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ITGA7 Gene Myopathy due to Integrin 7A deficiency
Test Details

ITGA7 gene myopathy is a rare genetic disorder caused by mutations in the ITGA7 gene. This gene provides instructions for making a protein called integrin alpha-7 (7). Integrins are a group of proteins that are involved in cell adhesion and signaling processes.

Integrin alpha-7 is mainly found in skeletal and cardiac muscle cells, where it plays a crucial role in maintaining the structural integrity and function of these muscles. Mutations in the ITGA7 gene can lead to a deficiency or dysfunction of integrin alpha-7, resulting in muscle weakness and wasting.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the identification of mutations or variations in the DNA sequence of specific genes, including the ITGA7 gene.

NGS genetic testing for ITGA7 gene myopathy can help confirm a diagnosis and identify the specific genetic mutation causing the condition. This information can be important for understanding the underlying cause of the disease, predicting disease progression, and guiding treatment decisions.

If you suspect that you or someone you know may have ITGA7 gene myopathy, it is recommended to consult with a healthcare professional or a genetic counselor who can provide more information about the testing process and help interpret the results.

SKU: TEST-1788 Category:

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