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MPDZ Gene Hydrocephalus Nonsyndromic Autosomal Recessive Type 2 Genetic Test

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

-21%

The “MPDZ Gene Hydrocephalus Nonsyndromic Autosomal Recessive Type 2 Genetic Test” is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the MPDZ gene, which have been linked to the development of nonsyndromic autosomal recessive type 2 hydrocephalus. Hydrocephalus is a condition characterized by an abnormal accumulation of cerebrospinal fluid (CSF) within the ventricles of the brain, which can lead to increased intracranial pressure, and in severe cases, brain damage. The condition described as nonsyndromic does not present with other syndromic features, making genetic testing crucial for accurate diagnosis.

The MPDZ gene plays a significant role in cellular functions that are critical for brain development and the regulation of fluid channels, which, when mutated, can disrupt normal CSF flow, leading to hydrocephalus. The genetic test involves analyzing the patient’s DNA to detect mutations in the MPDZ gene that are responsible for this specific type of hydrocephalus. This test is particularly important for families with a history of the condition, as it follows an autosomal recessive inheritance pattern, meaning that two copies of the mutated gene (one from each parent) are necessary for a child to be affected.

DNA Labs UAE offers this genetic test at a cost of 4400 AED. The test is conducted in their state-of-the-art laboratory facilities, where they utilize the latest in genetic testing technology to ensure accurate and reliable results. This test not only aids in the diagnosis of affected individuals but also provides crucial information for families regarding future pregnancies and the risk of recurrence of the condition. Additionally, early diagnosis through genetic testing can facilitate timely intervention and management of the condition, potentially improving outcomes for those affected.

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MPDZ Gene Hydrocephalus Nonsyndromic Autosomal Recessive Type 2 Genetic Test

At DNA Labs UAE, we offer the MPDZ Gene Hydrocephalus Nonsyndromic Autosomal Recessive Type 2 Genetic Test. This test is designed to diagnose and identify the genetic cause of hydrocephalus, specifically the nonsyndromic autosomal recessive type 2 form.

Test Components and Price

  • Test Name: MPDZ Gene Hydrocephalus Nonsyndromic Autosomal Recessive Type 2 Genetic Test
  • 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

Before undergoing the MPDZ Gene Hydrocephalus Nonsyndromic Autosomal Recessive Type 2 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by MPDZ Gene Hydrocephalus Nonsyndromic Autosomal Recessive Type 2.

About Hydrocephalus and the MPDZ Gene

Hydrocephalus is a condition characterized by the accumulation of cerebrospinal fluid in the brain, resulting in increased intracranial pressure and ventricle enlargement. The MPDZ gene is associated with the nonsyndromic autosomal recessive type 2 form of hydrocephalus.

NGS Technology and Genetic Testing

NGS (Next-Generation Sequencing) technology is utilized in the MPDZ Gene Hydrocephalus Nonsyndromic Autosomal Recessive Type 2 Genetic Test. This advanced method allows for the simultaneous analysis of multiple genes, providing a comprehensive evaluation of an individual’s genetic makeup. In the context of hydrocephalus, NGS can detect mutations or variations in the MPDZ gene that may be responsible for the development of the condition.

Nonsyndromic Autosomal Recessive Type 2 Hydrocephalus

Nonsyndromic autosomal recessive type 2 hydrocephalus refers to a specific form of hydrocephalus that is not associated with other abnormalities or syndromes. It is inherited in an autosomal recessive manner, meaning that both copies of the mutated MPDZ gene must be inherited, one from each parent, for the condition to develop.

Diagnostic and Carrier Testing

NGS genetic testing for MPDZ gene mutations can aid in diagnosing individuals with hydrocephalus, particularly in cases where the cause is unknown. It can also be used for carrier testing in families with a history of autosomal recessive hydrocephalus to determine if individuals are carriers of the mutated gene.

Importance of Genetic Counseling

It is important to note that NGS genetic testing is just one tool in the diagnostic process and should be interpreted alongside other clinical findings and family history. Genetic counseling is recommended before and after testing to provide individuals and families with a better understanding of the implications of the results.

Test Name MPDZ Gene Hydrocephalus nonsyndromic autosomal recessive type 2 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 MPDZ Gene Hydrocephalus, nonsyndromic, autosomal recessive type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MPDZ Gene Hydrocephalus, nonsyndromic, autosomal recessive type 2
Test Details

The MPDZ gene is associated with nonsyndromic autosomal recessive type 2 hydrocephalus. Hydrocephalus is a condition characterized by the accumulation of cerebrospinal fluid in the brain, leading to increased intracranial pressure and enlargement of the ventricles.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive evaluation of an individual’s genetic makeup. In the context of hydrocephalus, NGS can be used to identify mutations or variations in the MPDZ gene that may be responsible for the development of the condition.

Nonsyndromic autosomal recessive type 2 hydrocephalus refers to a specific form of hydrocephalus that is not associated with other abnormalities or syndromes. It is inherited in an autosomal recessive manner, meaning that an affected individual must inherit two copies of the mutated MPDZ gene, one from each parent, to develop the condition.

NGS genetic testing for MPDZ gene mutations can be helpful in diagnosing individuals with hydrocephalus, particularly in cases where the cause is unknown. It can also be used for carrier testing in families with a history of autosomal recessive hydrocephalus to determine if individuals are carriers of the mutated gene.

It is important to note that NGS genetic testing is just one tool in the diagnostic process and should be interpreted in conjunction with other clinical findings and family history. Genetic counseling is recommended before and after testing to provide individuals and families with a better understanding of the implications of the results.