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FAM111A Gene Kenny-Caffey syndrome type 2 Genetic Test

4,400 د.إ

-21%

The FAM111A Gene Kenny-Caffey Syndrome Type 2 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the FAM111A gene, which are associated with Kenny-Caffey Syndrome Type 2 (KCS2). KCS2 is a rare genetic disorder characterized by growth retardation, cortical thickening of tubular bones, delayed closure of the fontanelles, and hypocalcemia with normal parathyroid hormone levels. The condition is inherited in an autosomal dominant manner, meaning a mutation in just one of the two copies of the gene is sufficient to cause the disorder.

This genetic test involves analyzing the patient’s DNA to detect mutations in the FAM111A gene, providing essential information for the accurate diagnosis and management of Kenny-Caffey Syndrome Type 2. Early diagnosis through genetic testing can facilitate timely intervention, including management of symptoms and counseling for families regarding the risk of passing the condition to future generations.

The test is conducted at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates, known for its state-of-the-art facilities and expertise in genetic diagnostics. The cost of the FAM111A Gene Kenny-Caffey Syndrome Type 2 Genetic Test is 4400 AED, reflecting the comprehensive analysis and detailed reporting provided by the lab to ensure accurate diagnosis and optimal patient care.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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FAM111A Gene Kenny-Caffey Syndrome Type 2 Genetic Test

At DNA Labs UAE, we offer the FAM111A Gene Kenny-Caffey syndrome type 2 Genetic Test at a cost of AED 4400.0.

Test Details

The FAM111A gene is associated with Kenny-Caffey syndrome type 2, a rare genetic disorder characterized by skeletal abnormalities and developmental delay. Our NGS (Next Generation Sequencing) genetic testing method allows us to analyze multiple genes simultaneously.

In the context of Kenny-Caffey syndrome type 2, our NGS genetic testing can identify any mutations or variations in the FAM111A gene that may be responsible for the disorder. To conduct this test, we require a sample of the individual’s DNA, which can be obtained through a blood or saliva sample.

Using NGS technology, we sequence the DNA to identify any variations or mutations in the FAM111A gene. The results of the test can confirm a diagnosis of Kenny-Caffey syndrome type 2 and provide information about the specific genetic variant involved.

Our NGS genetic testing can help in providing a more accurate diagnosis, guiding treatment decisions, and informing genetic counseling for affected individuals and their families. Additionally, the results can contribute to research efforts aimed at better understanding the genetic basis of Kenny-Caffey syndrome type 2 and potentially developing targeted therapies in the future.

Test Components and Price

Test Name: FAM111A Gene Kenny-Caffey syndrome type 2 Genetic Test

Components: NGS Technology

Price: AED 4400.0

Sample Condition

We accept the following sample conditions for the FAM111A Gene Kenny-Caffey syndrome type 2 Genetic Test:

  • Blood
  • Extracted DNA
  • One drop of blood on FTA Card

Report Delivery

The report for the FAM111A Gene Kenny-Caffey syndrome type 2 Genetic Test will be delivered within 3 to 4 weeks.

Test Type and Doctor

Test Type: Neurological Disorders

Doctor: Neurologist

Test Department

The FAM111A Gene Kenny-Caffey syndrome type 2 Genetic Test is conducted in our Genetics department.

Pre Test Information

Prior to the FAM111A Gene Kenny-Caffey syndrome type 2 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with FAM111A Gene Kenny-Caffey syndrome type 2.

Test Name FAM111A Gene Kenny-Caffey syndrome type 2 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 FAM111A Gene Kenny-Caffey syndrome type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FAM111A Gene Kenny-Caffey syndrome type 2
Test Details

The FAM111A gene is associated with Kenny-Caffey syndrome type 2, which is a rare genetic disorder characterized by skeletal abnormalities and developmental delay.

NGS (Next Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Kenny-Caffey syndrome type 2, NGS genetic testing can be used to identify any mutations or variations in the FAM111A gene that may be responsible for the disorder.

This type of genetic testing involves obtaining a sample of the individual’s DNA, usually through a blood or saliva sample. The DNA is then sequenced using NGS technology to identify any variations or mutations in the FAM111A gene. The results of the test can help confirm a diagnosis of Kenny-Caffey syndrome type 2 and provide information about the specific genetic variant involved.

NGS genetic testing can be helpful in providing a more accurate diagnosis, guiding treatment decisions, and informing genetic counseling for affected individuals and their families. It can also contribute to research efforts aimed at better understanding the genetic basis of Kenny-Caffey syndrome type 2 and potentially developing targeted therapies in the future.