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USP9X Gene Mental Retardation X-Linked Type 99 Genetic Test Cost

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

-21%

The USP9X Gene Mental Retardation X-Linked Type 99 Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the USP9X gene, which have been associated with X-linked mental retardation type 99. This condition, primarily affecting males due to its X-linked inheritance pattern, is characterized by intellectual disabilities, developmental delays, and sometimes physical abnormalities. The genetic test involves analyzing the patient’s DNA to detect any alterations in the USP9X gene that could lead to the condition. With a cost of 4400 AED, this test is crucial for families seeking to understand the genetic underpinnings of intellectual disabilities and for guiding future healthcare and support plans. DNA Labs UAE employs state-of-the-art genetic testing technologies to ensure accurate and reliable results for patients and their families.

Description

USP9X Gene Mental Retardation X-linked Type 99 Genetic Test

Test Name: USP9X Gene Mental retardation X-linked type 99 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 USP9X Gene Mental retardation, X-linked type 99 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with USP9X Gene Mental retardation, X-linked type 99.

Test Details:

The USP9X gene is associated with a condition called mental retardation, X-linked type 99 (MRX99). This is a genetic disorder that primarily affects males and is characterized by intellectual disability or developmental delay.

NGS (Next-Generation Sequencing) genetic testing refers to a method used to analyze a person’s DNA sequence. It is a high-throughput technology that allows for the simultaneous sequencing of multiple genes or even the entire genome.

In the context of MRX99, NGS genetic testing can be used to identify mutations or variations in the USP9X gene that may be responsible for the condition. By analyzing the DNA sequence of the USP9X gene, NGS genetic testing can provide valuable information about the presence or absence of genetic abnormalities that may contribute to mental retardation or developmental delay in individuals.

This information can be helpful in diagnosing the condition, understanding its underlying genetic cause, and potentially guiding treatment or management strategies.

Test Name	USP9X Gene Mental retardation X-linked type 99 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 USP9X Gene Mental retardation, X-linked type 99 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with USP9X Gene Mental retardation, X-linked type 99
Test Details	The USP9X gene is associated with a condition called mental retardation, X-linked type 99 (MRX99). This is a genetic disorder that primarily affects males and is characterized by intellectual disability or developmental delay. NGS (Next-Generation Sequencing) genetic testing refers to a method used to analyze a person’s DNA sequence. It is a high-throughput technology that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of MRX99, NGS genetic testing can be used to identify mutations or variations in the USP9X gene that may be responsible for the condition. By analyzing the DNA sequence of the USP9X gene, NGS genetic testing can provide valuable information about the presence or absence of genetic abnormalities that may contribute to mental retardation or developmental delay in individuals. This information can be helpful in diagnosing the condition, understanding its underlying genetic cause, and potentially guiding treatment or management strategies.