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PHC1 Gene Microcephaly Autosomal Recessive Type 11 Genetic Test Cost

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

-21%

The PHC1 Gene Microcephaly Autosomal Recessive Type 11 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the PHC1 gene, which are implicated in Microcephaly Autosomal Recessive Type 11. This condition is characterized by significantly reduced head circumference, often accompanied by developmental delays and neurological issues, due to reduced brain size. The test is crucial for families with a history of the condition, aiming for early diagnosis and management strategies for affected individuals. The testing process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific genetic mutations associated with the disorder. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed genetic counseling that accompanies the results, guiding patients and families through the implications of the findings and potential next steps.

Home  Sample collection service available

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  • This test is not intended for medical diagnosis or treatment
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PHC1 Gene Microcephaly Autosomal Recessive Type 11 Genetic Test

At DNA Labs UAE, we offer the PHC1 Gene Microcephaly autosomal recessive type 11 Genetic Test. This test is designed to detect any mutations or variants in the PHC1 gene that may be causing microcephaly, autosomal recessive type 11.

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 PHC1 Gene Microcephaly autosomal recessive type 11 NGS Genetic DNA 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 who are affected by PHC1 Gene Microcephaly, autosomal recessive type 11 NGS Genetic DNA Test gene PHC1.

Test Details

The PHC1 gene is associated with a condition called microcephaly, autosomal recessive type 11. This condition is characterized by a smaller than average head size and is often accompanied by intellectual disability and delayed development.

NGS (Next-Generation Sequencing) genetic testing is used to analyze multiple genes simultaneously. In the case of microcephaly, autosomal recessive type 11, NGS genetic testing involves sequencing the PHC1 gene to identify any mutations or variants that may be causing the condition.

By identifying specific mutations in the PHC1 gene, NGS genetic testing can help confirm a diagnosis of microcephaly, autosomal recessive type 11 and provide information about the specific genetic cause of the condition. This information is valuable for genetic counseling, family planning, and potential development of targeted treatment strategies in the future.

Test Name PHC1 Gene Microcephaly autosomal recessive type 11 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 PHC1 Gene Microcephaly, autosomal recessive type 11 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PHC1 Gene Microcephaly, autosomal recessive type 11 NGS Genetic DNA Test gene PHC1
Test Details

The PHC1 gene is associated with a condition called microcephaly, autosomal recessive type 11. Microcephaly is a neurodevelopmental disorder characterized by a smaller than average head size and often associated with intellectual disability and delayed development.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of microcephaly, autosomal recessive type 11, NGS genetic testing would involve sequencing the PHC1 gene to identify any mutations or variants that may be causing the condition.

By identifying specific mutations in the PHC1 gene, NGS genetic testing can help confirm a diagnosis of microcephaly, autosomal recessive type 11 and provide information about the specific genetic cause of the condition. This information can be valuable for genetic counseling, family planning, and potentially for developing targeted treatment strategies in the future.

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