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RNF216 Gene Gordon Holmes Syndrome Genetic Test

4,400 د.إ

-21%

RNF216 Gene Gordon Holmes Syndrome Genetic Test is a specialized genetic assessment conducted at DNA Labs UAE, designed to diagnose Gordon Holmes syndrome, a rare neurological condition. This syndrome is characterized by a combination of cerebellar ataxia, which affects coordination and balance, and hypogonadotropic hypogonadism, a condition related to reproductive system development and function. The test specifically targets mutations in the RNF216 gene, which have been linked to the syndrome, providing crucial information for accurate diagnosis and management.

The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the lab for the presence of mutations in the RNF216 gene. This genetic insight is pivotal for families and individuals in understanding the condition, potential treatments, and implications for family planning.

The cost of the RNF216 Gene Gordon Holmes Syndrome Genetic Test at DNA Labs UAE is set at 4400 AED. This price reflects the comprehensive nature of the test, including the advanced genetic sequencing and analysis required to identify the specific gene mutations associated with Gordon Holmes syndrome. Individuals considering this test are advised to consult with a healthcare provider or genetic counselor to understand its benefits, limitations, and the significance of the results in the context of their personal health and family history.

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RNF216 Gene Gordon Holmes Syndrome Genetic Test

Welcome to DNA Labs UAE, where we offer the RNF216 Gene Gordon Holmes Syndrome Genetic Test. This test is designed to detect mutations in the RNF216 gene that may be responsible for Gordon Holmes syndrome. Read on to learn more about the components, cost, sample condition, report delivery, method, test type, doctor, and test department associated with this test.

Test Name: RNF216 Gene Gordon Holmes Syndrome Genetic Test

Components: RNF216 Gene Gordon Holmes Syndrome 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

Before undergoing the RNF216 Gene Gordon Holmes Syndrome NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by RNF216 Gene Gordon Holmes Syndrome.

Test Details

The RNF216 gene is associated with Gordon Holmes syndrome, a rare genetic disorder characterized by cerebellar ataxia, hypogonadotropic hypogonadism, and cognitive impairment. The RNF216 gene plays a role in protein degradation and the immune system.

NGS (Next-Generation Sequencing) genetic testing is a cutting-edge technology that allows for the simultaneous sequencing of multiple genes. This type of genetic testing is used to identify mutations in the RNF216 gene that may be linked to Gordon Holmes syndrome.

The RNF216 Gene Gordon Holmes Syndrome NGS genetic test is essential in diagnosing the condition, guiding treatment decisions, and assessing the risk of passing the syndrome to future generations.

For more information or to schedule an appointment for the RNF216 Gene Gordon Holmes Syndrome Genetic Test, please contact our Genetics Test Department and consult with our Neurologist.

 

Test NameRNF216 Gene Gordon Holmes Syndrome Genetic Test
Components 
Price4400.0 AED
Sample ConditionBlood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery3 to 4 Weeks
MethodNGS Technology
Test typeNeurological Disorders
DoctorNeurologist
Test Department:Genetics
Pre Test InformationClinical History of Patient who is going for RNF216 Gene Gordon Holmes Syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with RNF216 Gene Gordon Holmes Syndrome
Test Details

RNF216 gene is associated with Gordon Holmes syndrome, which is a rare genetic disorder characterized by the combination of cerebellar ataxia, hypogonadotropic hypogonadism, and cognitive impairment. The RNF216 gene provides instructions for making a protein that plays a role in the regulation of protein degradation and the immune system.

 

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced technology to sequence multiple genes simultaneously. It is used to identify genetic mutations that may be associated with certain diseases, including Gordon Holmes syndrome.

 

Therefore, RNF216 gene Gordon Holmes Syndrome NGS genetic test is a genetic test that examines the RNF216 gene for mutations that may cause Gordon Holmes syndrome using NGS technology. This test can help diagnose the condition, guide treatment decisions, and provide information about the risk of passing the condition to future generations.