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RAB39B Gene Mental Retardation X-Linked Type 72 Genetic Test

3,200 د.إ

-43%

The RAB39B gene mental retardation X-linked type 72 genetic test is a specialized diagnostic procedure aimed at detecting mutations in the RAB39B gene, which have been linked to a form of X-linked intellectual disability. This condition is characterized by various degrees of cognitive impairment, and in some cases, it may be accompanied by other neurological or physical abnormalities. The RAB39B gene plays a critical role in neuronal development and function, and mutations in this gene can disrupt normal brain development and cognitive processes.

The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to identify any mutations in the RAB39B gene. This test is crucial for families with a history of X-linked intellectual disability, as it can provide a definitive diagnosis, guide treatment and management options, and offer insights into the risk of passing the condition to future generations.

The cost of the RAB39B gene mental retardation X-linked type 72 genetic test at DNA Labs UAE is 3200 AED. While the price may seem steep, the information it provides can be invaluable for affected individuals and their families, enabling them to make informed decisions about their health and wellbeing.

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RAB39B Gene Mental retardation X-linked type 72 Genetic Test

Components: RAB39B Gene Mental retardation X-linked type 72 Genetic Test

Price: 3200.0 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 RAB39B Gene Mental retardation, X-linked type 72 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAB39B Gene Mental retardation, X-linked type 72

Test Details:

The RAB39B gene is associated with a condition called Mental Retardation, X-linked type 72 (MRX72). This is a genetic disorder characterized by intellectual disability, developmental delays, and other neurological problems.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual. It allows for the simultaneous analysis of multiple genes or even the entire exome or genome. In the context of MRX72, NGS genetic testing can be used to identify mutations or variations in the RAB39B gene that may be responsible for the condition. By analyzing the DNA sequence, NGS testing can provide valuable information about the presence or absence of mutations in the RAB39B gene, helping in the diagnosis of MRX72. This information can also be used for genetic counseling, assessing the risk of the condition in family members, and potentially guiding treatment decisions.

Test Name RAB39B Gene Mental retardation X-linked type 72 Genetic Test
Components
Price 3200.0 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 RAB39B Gene Mental retardation, X-linked type 72 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with RAB39B Gene Mental retardation, X-linked type 72
Test Details

The RAB39B gene is associated with a condition called Mental Retardation, X-linked type 72 (MRX72). This is a genetic disorder characterized by intellectual disability, developmental delays, and other neurological problems.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual. It allows for the simultaneous analysis of multiple genes or even the entire exome or genome. In the context of MRX72, NGS genetic testing can be used to identify mutations or variations in the RAB39B gene that may be responsible for the condition.

By analyzing the DNA sequence, NGS testing can provide valuable information about the presence or absence of mutations in the RAB39B gene, helping in the diagnosis of MRX72. This information can also be used for genetic counseling, assessing the risk of the condition in family members, and potentially guiding treatment decisions.