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INPPL1 Gene Opsismodysplasia Genetic Test Cost

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

-21%

The INPPL1 gene opsismodysplasia genetic test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the INPPL1 gene, which are known to cause opsismodysplasia. Opsismodysplasia is a rare skeletal disorder characterized by short stature, facial abnormalities, and skeletal malformations. The condition is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

The test is particularly crucial for families with a history of the condition or for individuals showing symptoms, as early diagnosis can lead to better management of the disorder. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any abnormalities in the INPPL1 gene.

DNA Labs UAE, a reputable facility known for its advanced genetic testing services, offers this test at a cost of 4400 AED. The price reflects the sophisticated technology and expertise required to accurately identify mutations in the INPPL1 gene. Upon completion of the test, patients receive a comprehensive report detailing the findings, which can be a valuable tool for healthcare providers in developing an appropriate treatment and management plan for those affected by opsismodysplasia.

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INPPL1 Gene Opsismodysplasia Genetic Test

Cost: AED 4400.0

Are you or your loved ones experiencing symptoms such as short stature, facial abnormalities, and skeletal deformities? It could be a result of a rare genetic disorder called opsismodysplasia. At DNA Labs UAE, we offer the INPPL1 Gene Opsismodysplasia Genetic Test to help diagnose this condition.

Test Components:

  • Price: AED 4400.0
  • 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

Test Department: Genetics

Our team of dermatologists specializing in genetics will conduct the INPPL1 Gene Opsismodysplasia Genetic Test.

Pre Test Information:

Before the test, it is important to provide the clinical history of the patient who is going for the INPPL1 Gene Opsismodysplasia NGS Genetic DNA Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the INPPL1 Gene Opsismodysplasia NGS Genetic DNA Test gene INPPL1.

Test Details:

The INPPL1 gene is associated with opsismodysplasia, a rare genetic disorder characterized by short stature, facial abnormalities, and skeletal deformities. This condition is autosomal recessive, meaning that both parents must pass on a mutated copy of the INPPL1 gene for the individual to develop the disorder.

Our NGS (Next-Generation Sequencing) genetic testing utilizes advanced sequencing technologies to analyze multiple genes simultaneously. In the case of opsismodysplasia, NGS genetic testing can identify mutations or variations in the INPPL1 gene, confirming a diagnosis.

NGS genetic testing provides valuable information about an individual’s genetic makeup, aiding in the diagnosis and management of genetic disorders. It also enables genetic counseling and assessment of the risk of passing on the condition to future generations.

If you suspect opsismodysplasia or want to explore your genetic makeup, contact DNA Labs UAE today to schedule an appointment for the INPPL1 Gene Opsismodysplasia Genetic Test.

Test Name INPPL1 Gene Opsismodysplasia 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 INPPL1 Gene Opsismodysplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with INPPL1 Gene Opsismodysplasia NGS Genetic DNA Test gene INPPL1
Test Details

The INPPL1 gene is associated with a rare genetic disorder called opsismodysplasia. Opsismodysplasia is a skeletal dysplasia characterized by short stature, facial abnormalities, and skeletal deformities. It is an autosomal recessive disorder, meaning that an individual must inherit two copies of the mutated INPPL1 gene (one from each parent) to develop the condition.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of opsismodysplasia, NGS genetic testing can be used to identify mutations or variations in the INPPL1 gene, helping to confirm a diagnosis.

NGS genetic testing can provide valuable information about an individual’s genetic makeup and can be useful in diagnosing and managing genetic disorders. It can also help in providing genetic counseling and assessing the risk of passing on the condition to future generations.

SKU: TEST-3170 Category:

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