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OFD1 Gene Joubert Syndrome Type 10 Genetic Test

4,400 د.إ

-21%

The OFD1 Gene Joubert Syndrome Type 10 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the OFD1 gene, which are associated with Joubert Syndrome Type 10. This condition is a rare genetic disorder characterized by the underdevelopment of the cerebellum and brain stem, leading to a range of neurological symptoms, including coordination and balance issues, abnormal eye movements, and developmental delays. The test plays a crucial role in the early diagnosis and management of the syndrome, allowing for targeted interventions and support to improve the quality of life for affected individuals. Priced at 4400 AED, this test is a valuable resource for families seeking answers to complex genetic questions, providing them with critical information on their genetic health and predispositions.

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OFD1 Gene Joubert Syndrome Type 10 Genetic Test

Test Details

The OFD1 gene is associated with Joubert syndrome type 10. Joubert syndrome is a rare genetic disorder that affects the development of the brainstem and cerebellum, leading to various symptoms such as intellectual disability, breathing abnormalities, and characteristic facial features.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Joubert syndrome type 10, NGS genetic testing can be used to identify mutations or variations in the OFD1 gene that may be responsible for the condition.

NGS genetic testing can provide valuable information for diagnosis, prognosis, and genetic counseling for individuals suspected of having Joubert syndrome type 10. It can help confirm the diagnosis, identify specific genetic variants, and provide information about the inheritance pattern of the condition.

It is important to consult with a healthcare professional or genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Joubert syndrome type 10 in specific cases. They can provide guidance on the testing process, interpretation of results, and implications for individuals and their families.

Test Name

OFD1 Gene Joubert Syndrome Type 10 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

Neurological Disorders

Doctor

Neurologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for OFD1 Gene Joubert Syndrome Type 10 NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with OFD1 Gene Joubert Syndrome Type 10

Test Name OFD1 Gene Joubert syndrome type 10 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 OFD1 Gene Joubert syndrome type 10 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with OFD1 Gene Joubert syndrome type 10
Test Details

The OFD1 gene is associated with Joubert syndrome type 10. Joubert syndrome is a rare genetic disorder that affects the development of the brainstem and cerebellum, leading to various symptoms such as intellectual disability, breathing abnormalities, and characteristic facial features.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Joubert syndrome type 10, NGS genetic testing can be used to identify mutations or variations in the OFD1 gene that may be responsible for the condition.

NGS genetic testing can provide valuable information for diagnosis, prognosis, and genetic counseling for individuals suspected of having Joubert syndrome type 10. It can help confirm the diagnosis, identify specific genetic variants, and provide information about the inheritance pattern of the condition.

It is important to consult with a healthcare professional or genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Joubert syndrome type 10 in specific cases. They can provide guidance on the testing process, interpretation of results, and implications for individuals and their families.