MECP2 Gene Rett Syndrome Genetic Test

Are you concerned about Rett syndrome? DNA Labs UAE offers the MECP2 Gene Rett Syndrome Genetic Test to help diagnose this rare genetic disorder. In this blog, we will discuss the symptoms, diagnosis process, cost, and other important details about this test.

Test Name: MECP2 Gene Rett Syndrome 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

Dysmorphology

Doctor

Pediatrics

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for MECP2 Gene Rett Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MECP2 Gene Rett Syndrome NGS Genetic DNA Test gene MECP2.

About Rett Syndrome and the MECP2 Gene

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

The Role of NGS Technology in Genetic Testing

NGS, or next-generation sequencing, is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of Rett syndrome, NGS can be used to analyze the MECP2 gene for mutations or variations that may be responsible for the disorder.

NGS-based genetic testing for Rett syndrome involves sequencing the MECP2 gene from a patient’s DNA sample. This can be done using various techniques, such as targeted gene panels or whole-exome sequencing. The sequencing data is then analyzed to identify any mutations or variations in the MECP2 gene that may be associated with Rett syndrome.

Benefits of NGS-based Genetic Testing for Rett Syndrome

NGS-based genetic testing for Rett syndrome can provide valuable information for diagnosis, prognosis, and genetic counseling. It can help confirm a diagnosis of Rett syndrome in individuals with clinical symptoms and can also identify carriers of MECP2 mutations in family members.

It’s important to note that while MECP2 mutations are the most common cause of Rett syndrome, not all individuals with Rett syndrome will have a detectable MECP2 mutation. In some cases, other genes or genetic factors may be involved. Therefore, a negative NGS test for MECP2 mutations does not rule out a diagnosis of Rett syndrome.

If you suspect Rett syndrome or have a family history of the disorder, consider getting the MECP2 Gene Rett Syndrome Genetic Test at DNA Labs UAE. Our expert team of geneticists and pediatricians will provide you with accurate and reliable results.