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MAN1B1 Gene Mental Retardation Autosomal Recessive Type 15 Genetic Test

4,400 د.إ

-21%

The MAN1B1 gene is associated with a condition known as Mental Retardation, Autosomal Recessive Type 15 (MRT15). This rare genetic disorder is characterized by intellectual disabilities and, in some cases, physical abnormalities. The condition is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the altered gene, one from each parent, to be affected.

DNA Labs UAE offers a genetic test specifically designed to identify mutations in the MAN1B1 gene, which can confirm a diagnosis of MRT15. This test is crucial for families seeking answers about intellectual disabilities and for guiding potential treatment and management strategies. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, and then analyzing the genetic material for specific mutations associated with the condition.

The cost of the MAN1B1 Gene Mental Retardation Autosomal Recessive Type 15 Genetic Test at DNA Labs UAE is 4400 AED. This price includes the full process of sample collection, genetic analysis, and a comprehensive report of the findings. The results of this test can provide essential information for affected individuals and their families, including the confirmation of a diagnosis, insights into the condition, and information relevant to family planning.

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MAN1B1 Gene Mental Retardation Autosomal Recessive Type 15 Genetic Test

At DNA Labs UAE, we offer the MAN1B1 Gene Mental Retardation Autosomal Recessive Type 15 Genetic Test. This test helps diagnose a specific type of mental retardation known as autosomal recessive type 15, which is characterized by intellectual disability, delayed speech development, and various physical abnormalities.

Test Components

  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery

The report will be delivered within 3 to 4 weeks.

Method

We use NGS (Next-Generation Sequencing) technology to analyze the DNA sequence of the MAN1B1 gene.

Test Type

This test falls under the category of Neurological Disorders.

Referring Doctor

This test is recommended by Neurologists.

Test Department

This test is conducted in our Genetics department.

Pre Test Information

Prior to the test, we require the clinical history of the patient who is going for the MAN1B1 Gene Mental Retardation Autosomal Recessive Type 15 NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by this genetic disorder.

Test Details

The MAN1B1 gene, also known as Mannosidase alpha class 1B member 1 gene, is associated with autosomal recessive type 15 mental retardation. NGS genetic testing is used to analyze the DNA sequence of an individual’s genes, including the MAN1B1 gene. This test helps in diagnosing genetic disorders, such as autosomal recessive type 15, by identifying any abnormalities or mutations in the MAN1B1 gene. By analyzing the MAN1B1 gene through NGS testing, healthcare professionals can provide a more accurate diagnosis, determine the inheritance pattern, and offer appropriate genetic counseling and management strategies for individuals and their families affected by autosomal recessive type 15.

Test Name MAN1B1 Gene Mental retardation autosomal recessive type 15 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 MAN1B1 Gene Mental retardation, autosomal recessive type 15 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MAN1B1 Gene Mental retardation, autosomal recessive type 15
Test Details

MAN1B1 gene, also known as Mannosidase alpha class 1B member 1 gene, is associated with a specific type of mental retardation known as autosomal recessive type 15. This genetic disorder is characterized by intellectual disability, delayed speech development, and various physical abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the identification of specific mutations or variations in genes, including the MAN1B1 gene. NGS testing can help diagnose genetic disorders, including autosomal recessive type 15, by detecting any abnormalities or mutations in the MAN1B1 gene.

By analyzing the MAN1B1 gene through NGS testing, healthcare professionals can provide a more accurate diagnosis, determine the inheritance pattern, and offer appropriate genetic counseling and management strategies for individuals and their families affected by autosomal recessive type 15.