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MECP2 Gene Rett Syndrome Preserved Speech Variant Genetic Test Cost

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

-21%

The MECP2 gene Rett Syndrome Preserved Speech Variant (PSV) genetic test is a specialized diagnostic tool designed to identify mutations in the MECP2 gene, which are linked to a rare form of Rett Syndrome where individuals retain the ability to speak. This variant of Rett Syndrome, while sharing many characteristics with classic Rett Syndrome, allows for some degree of verbal communication, making its identification crucial for tailored care and intervention strategies.

Performed at DNA Labs UAE, the test involves analyzing the patient’s DNA to detect abnormalities in the MECP2 gene. These abnormalities can provide conclusive evidence of the PSV of Rett Syndrome, enabling healthcare providers to make accurate diagnoses. Early diagnosis is key to managing symptoms and improving the quality of life for those affected.

The cost of the MECP2 gene Rett Syndrome Preserved Speech Variant genetic test is 4400 AED. This investment covers the comprehensive analysis required to detect the specific gene mutations associated with this condition. Given the specialized nature of this test and its potential to significantly impact patient care, it represents a critical step for families seeking answers about this particular variant of Rett Syndrome.

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MECP2 Gene Rett Syndrome Preserved Speech Variant Genetic Test

At DNA Labs UAE, we offer the MECP2 Gene Rett Syndrome Preserved Speech Variant Genetic Test at a cost of AED 4400.0.

Test Components

The test includes:

  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery

Reports are delivered within 3 to 4 weeks.

Method

We use NGS (Next-Generation Sequencing) technology for this genetic test.

Test Type

This test is specifically designed for neurological disorders.

Doctor

Our qualified neurologists will oversee the testing process.

Test Department

This test is conducted by our Genetics department.

Pre Test Information

Prior to the test, we recommend a genetic counseling session to gather clinical history and draw a pedigree chart of family members affected by MECP2 Gene Rett Syndrome Preserved Speech Variant.

Test Details

The MECP2 gene is associated with Rett syndrome, a rare genetic disorder that mainly affects females. Rett syndrome is characterized by severe cognitive and physical impairments, loss of purposeful hand skills, and the development of repetitive hand movements.

However, there is a variant of Rett syndrome called the preserved speech variant, where affected individuals have some degree of preserved speech and cognitive abilities.

NGS genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Rett syndrome, NGS genetic testing can be used to analyze the MECP2 gene for mutations or variations that may be associated with the preserved speech variant.

NGS genetic testing can help confirm a diagnosis of Rett syndrome and provide information about the specific genetic variant present in an individual. This information can be valuable for understanding the prognosis, potential treatment options, and recurrence risk for affected individuals and their families.

It is important to note that genetic testing for Rett syndrome, including the preserved speech variant, should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

Test Name MECP2 Gene Rett syndrome preserved speech variant 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 MECP2 Gene Rett syndrome preserved speech variant NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MECP2 Gene Rett syndrome preserved speech variant
Test Details

The MECP2 gene is associated with Rett syndrome, a rare genetic disorder that predominantly affects females. Rett syndrome is characterized by severe cognitive and physical impairments, loss of purposeful hand skills, and the development of repetitive hand movements. However, there is a variant of Rett syndrome called the preserved speech variant, where affected individuals have some degree of preserved speech and cognitive abilities.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Rett syndrome, NGS genetic testing can be used to analyze the MECP2 gene for mutations or variations that may be associated with the preserved speech variant.

NGS genetic testing can help confirm a diagnosis of Rett syndrome and provide information about the specific genetic variant present in an individual. This information can be valuable for understanding the prognosis, potential treatment options, and recurrence risk for affected individuals and their families.

It is important to note that genetic testing for Rett syndrome, including the preserved speech variant, should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

SKU: TEST-1956 Category:

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