FAM111A Gene Gracile bone dysplasia Genetic Test sale cost 4400 AED
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FAM111A Gene Gracile bone dysplasia Genetic Test Cost

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

-21%

The FAM111A gene plays a critical role in the development and maintenance of bones, and mutations in this gene can lead to gracile bone dysplasia, a rare genetic disorder characterized by thin, fragile bones that are prone to fractures. To diagnose this condition, a genetic test targeting the FAM111A gene is available, offering a definitive way to identify mutations associated with gracile bone dysplasia. This test is particularly important for families with a history of the condition or for individuals presenting symptoms suggestive of the disorder.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test provides a comprehensive analysis of the FAM111A gene to detect any abnormalities that could indicate the presence of gracile bone dysplasia. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed using advanced genetic sequencing technologies to identify mutations in the FAM111A gene.

The cost of the FAM111A gene test for gracile bone dysplasia at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expertise required to accurately detect and interpret mutations in the gene. Upon completion of the test, patients receive a detailed report that explains the findings and, if a mutation is detected, outlines the implications for the patient’s health and potential treatment or management options. This information can be crucial for making informed decisions about care and for understanding the risk of passing the condition on to future generations.

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FAM111A Gene Gracile bone dysplasia Genetic Test

Welcome to DNA Labs UAE, your trusted genetic testing lab in the UAE. In this blog post, we will be discussing the FAM111A Gene Gracile bone dysplasia Genetic Test, its cost, symptoms, diagnosis, and more.

Test Name: FAM111A Gene Gracile bone dysplasia 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: Osteology Dermatology Immunology Disorders

Doctor: Dermatologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for FAM111A Gene Gracile bone dysplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FAM111A Gene Gracile bone dysplasia NGS Genetic DNA Test gene FAM111A

Test Details

The FAM111A gene is associated with a rare genetic disorder called gracile bone dysplasia. Gracile bone dysplasia is characterized by skeletal abnormalities, including thin and fragile bones, shortened limbs, and joint deformities. This condition is inherited in an autosomal recessive manner, meaning that both copies of the FAM111A gene must be mutated for the disorder to be present.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the context of gracile bone dysplasia, NGS genetic testing can be used to identify mutations in the FAM111A gene. This test involves sequencing the entire coding region of the gene to identify any genetic variants or mutations that may be responsible for the disorder.

NGS genetic testing is a powerful tool that can provide a comprehensive analysis of multiple genes, allowing for a more accurate diagnosis and potentially identifying other genetic variants that may be contributing to the condition. It can also be used for carrier testing to determine if an individual carries a mutation in the FAM111A gene, even if they do not show any symptoms of gracile bone dysplasia.

Overall, NGS genetic testing for the FAM111A gene can aid in the diagnosis, management, and genetic counseling of individuals with gracile bone dysplasia and their families.

Test Name FAM111A Gene Gracile bone dysplasia 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FAM111A Gene Gracile bone dysplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FAM111A Gene Gracile bone dysplasia NGS Genetic DNA Test gene FAM111A
Test Details

FAM111A gene is associated with a rare genetic disorder called gracile bone dysplasia. Gracile bone dysplasia is characterized by skeletal abnormalities, including thin and fragile bones, shortened limbs, and joint deformities. This condition is inherited in an autosomal recessive manner, meaning that both copies of the FAM111A gene must be mutated for the disorder to be present.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the context of gracile bone dysplasia, NGS genetic testing can be used to identify mutations in the FAM111A gene. This test involves sequencing the entire coding region of the gene to identify any genetic variants or mutations that may be responsible for the disorder.

NGS genetic testing is a powerful tool that can provide a comprehensive analysis of multiple genes, allowing for a more accurate diagnosis and potentially identifying other genetic variants that may be contributing to the condition. It can also be used for carrier testing to determine if an individual carries a mutation in the FAM111A gene, even if they do not show any symptoms of gracile bone dysplasia.

Overall, NGS genetic testing for the FAM111A gene can aid in the diagnosis, management, and genetic counseling of individuals with gracile bone dysplasia and their families.

SKU: TEST-3002 Category:

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