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KNL1 Gene Microcephaly Autosomal Recessive Type 4 Genetic Test Cost

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

-21%

The KNL1 gene plays a crucial role in cell division and is associated with Microcephaly Autosomal Recessive Type 4 (MCPH4), a genetic condition characterized by a significantly smaller head size compared to individuals of the same age and sex. This condition often leads to developmental delays and neurological issues. The genetic test for MCPH4 through the analysis of the KNL1 gene is a critical step in diagnosing this condition, enabling healthcare providers to better understand the genetic makeup of the affected individual and to offer appropriate care and support.

Conducted at DNA Labs UAE, the test specifically looks for mutations in the KNL1 gene that are indicative of MCPH4. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, and analyzing the genetic material for specific mutations associated with the condition. This test is crucial for families with a history of microcephaly or genetic disorders, as it can provide vital information for family planning and management of the condition.

The cost of the KNL1 gene microcephaly autosomal recessive type 4 genetic test at DNA Labs UAE is 4400 AED. While the price might seem high, the test offers invaluable insights into the genetic disorder, facilitating early intervention and support for affected individuals and their families. It’s important for potential clients to consult with healthcare professionals to understand the implications of the test results and to receive guidance on the steps to take following diagnosis.

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KNL1 Gene Microcephaly Autosomal Recessive Type 4 Genetic Test

At DNA Labs UAE, we offer the KNL1 Gene Microcephaly Autosomal Recessive Type 4 Genetic Test. This test is designed to analyze the KNL1 gene, which is associated with microcephaly, a condition characterized by a smaller than average head size and impaired brain development.

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

Prior to undergoing the KNL1 Gene Microcephaly Autosomal Recessive Type 4 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 with KNL1 Gene Microcephaly Autosomal Recessive Type 4 NGS Genetic DNA Test gene KNL1.

Test Details

Autosomal recessive type 4 microcephaly refers to a specific subtype of microcephaly that is inherited in an autosomal recessive manner. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the analysis of multiple genes simultaneously.

In the context of microcephaly, NGS testing can be used to analyze the KNL1 gene, along with other genes known to be associated with microcephaly. This helps identify potential genetic variants or mutations that may be causing the condition.

By identifying specific genetic variants or mutations in the KNL1 gene, NGS genetic testing can help confirm a diagnosis of microcephaly and provide valuable information for genetic counseling and family planning. It also aids in understanding the underlying molecular mechanisms of the condition and potentially guides the development of targeted therapies in the future.

Test Name KNL1 Gene Microcephaly autosomal recessive type 4 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 KNL1 Gene Microcephaly, autosomal recessive type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KNL1 Gene Microcephaly, autosomal recessive type 4 NGS Genetic DNA Test gene KNL1
Test Details

The KNL1 gene is associated with microcephaly, which is a condition characterized by a smaller than average head size and impaired brain development. Autosomal recessive type 4 microcephaly refers to a specific subtype of microcephaly that is inherited in an autosomal recessive manner.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the analysis of multiple genes simultaneously. In the context of microcephaly, NGS testing can be used to analyze the KNL1 gene, along with other genes known to be associated with microcephaly, to identify potential genetic variants or mutations that may be causing the condition.

By identifying specific genetic variants or mutations in the KNL1 gene, NGS genetic testing can help confirm a diagnosis of microcephaly and provide valuable information for genetic counseling and family planning. It can also aid in understanding the underlying molecular mechanisms of the condition and potentially guide the development of targeted therapies in the future.

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