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CDT1 Gene Meier-Gorlin Syndrome Type 4 Genetic Test

4,400 د.إ

-21%

The CDT1 gene Meier-Gorlin syndrome type 4 genetic test is a specialized diagnostic examination aimed at identifying mutations in the CDT1 gene, which are associated with Meier-Gorlin syndrome type 4. Meier-Gorlin syndrome is a rare genetic disorder characterized by short stature, small ears, and absent or underdeveloped kneecaps. Type 4 of this syndrome specifically implicates mutations in the CDT1 gene, affecting the crucial process of DNA replication and cell cycle regulation, leading to the syndrome’s phenotypic manifestations.

This test is crucial for early diagnosis, allowing for appropriate management and treatment strategies to be implemented, enhancing the quality of life for affected individuals. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test ensures accuracy and reliability, employing advanced genetic sequencing technologies to detect mutations in the CDT1 gene.

The cost of the CDT1 gene Meier-Gorlin syndrome type 4 genetic test is 4400 AED, reflecting the comprehensive analysis and detailed reporting provided. This investment facilitates a deeper understanding of the genetic basis of the syndrome, offering affected families critical information for genetic counseling and future family planning decisions.

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CDT1 Gene Meier-Gorlin Syndrome Type 4 Genetic Test

Test Name: CDT1 Gene Meier-Gorlin Syndrome Type 4 Genetic Test

Components: NGS Technology

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 CDT1 Gene Meier-Gorlin Syndrome Type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CDT1 Gene Meier-Gorlin Syndrome Type 4 NGS Genetic DNA Test gene CDT1

Test Details

The CDT1 gene is associated with Meier-Gorlin Syndrome Type 4, a rare genetic disorder characterized by short stature, small ears, and absent or underdeveloped kneecaps. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of Meier-Gorlin Syndrome Type 4, NGS testing can be used to identify any mutations or variations in the CDT1 gene that may be causing the condition.

This type of testing can help confirm a diagnosis, provide information about the inheritance pattern, and assist in genetic counseling. NGS genetic testing involves collecting a sample of DNA, usually through a blood or saliva sample, and sequencing the DNA to identify any genetic variations. The results are then analyzed by genetic specialists to determine if there are any disease-causing mutations in the CDT1 gene.

It’s important to note that genetic testing for Meier-Gorlin Syndrome Type 4 may not be readily available at all healthcare facilities. A geneticist or genetic counselor can provide more information about the availability and appropriateness of this type of testing for an individual’s specific situation.

Test Name CDT1 Gene Meier-Gorlin syndrome 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 CDT1 Gene Meier-Gorlin syndrome type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CDT1 Gene Meier-Gorlin syndrome type 4 NGS Genetic DNA Test gene CDT1
Test Details

The CDT1 gene is associated with Meier-Gorlin syndrome type 4, a rare genetic disorder characterized by short stature, small ears, and absent or underdeveloped kneecaps.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of Meier-Gorlin syndrome type 4, NGS testing can be used to identify any mutations or variations in the CDT1 gene that may be causing the condition. This type of testing can help confirm a diagnosis, provide information about the inheritance pattern, and assist in genetic counseling.

NGS genetic testing involves collecting a sample of DNA, usually through a blood or saliva sample, and sequencing the DNA to identify any genetic variations. The results are then analyzed by genetic specialists to determine if there are any disease-causing mutations in the CDT1 gene.

It’s important to note that genetic testing for Meier-Gorlin syndrome type 4 may not be readily available at all healthcare facilities. A geneticist or genetic counselor can provide more information about the availability and appropriateness of this type of testing for an individual’s specific situation.

SKU: TEST-4231 Category:

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