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GPSM2 Gene Chudley-McCullough Syndrome Genetic Test Cost

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

-21%

The GPSM2 Gene Chudley-McCullough Syndrome Genetic Test is a specialized diagnostic tool used to identify mutations in the GPSM2 gene, which are associated with Chudley-McCullough Syndrome. This condition is a rare genetic disorder characterized by sensorineural hearing loss and brain abnormalities, potentially leading to developmental delays and other neurological issues. The test involves analyzing the patient’s DNA to detect specific genetic alterations in the GPSM2 gene that are indicative of the syndrome.

Performed at DNA Labs UAE, a leading facility in genetic testing and diagnostics, the test offers a reliable means for clinicians to diagnose Chudley-McCullough Syndrome accurately. The cost of the test is 4400 AED, reflecting the comprehensive analysis and expertise required to interpret the results accurately. Identifying the genetic basis of the syndrome through this test can significantly aid in managing the condition, allowing for targeted interventions and support for affected individuals and their families.

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GPSM2 Gene Chudley-McCullough Syndrome Genetic Test

Test Name: GPSM2 Gene Chudley-McCullough Syndrome Genetic Test

Components: GPSM2 gene analysis

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 GPSM2 Gene Chudley-McCullough Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GPSM2 Gene Chudley-McCullough Syndrome NGS Genetic DNA Test gene GPSM2.

Test Details

The GPSM2 gene is associated with a rare genetic disorder called Chudley-McCullough syndrome. This syndrome is characterized by a range of symptoms including intellectual disability, delayed development, seizures, and various physical abnormalities.

NGS (Next-Generation Sequencing) is a genetic testing method that can be used to analyze the DNA sequence of the GPSM2 gene. This test involves sequencing the DNA of an individual to identify any variations or mutations in the GPSM2 gene that may be causing or contributing to the symptoms of Chudley-McCullough syndrome.

By identifying specific genetic changes in the GPSM2 gene, NGS testing can help confirm a diagnosis of Chudley-McCullough syndrome and provide valuable information for genetic counseling, treatment planning, and management of the condition.

Test Name GPSM2 Gene Chudley-McCullough syndrome 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 GPSM2 Gene Chudley-McCullough syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GPSM2 Gene Chudley-McCullough syndrome NGS Genetic DNA Test gene GPSM2
Test Details

The GPSM2 gene is associated with a rare genetic disorder called Chudley-McCullough syndrome. This syndrome is characterized by a range of symptoms including intellectual disability, delayed development, seizures, and various physical abnormalities.

NGS (Next-Generation Sequencing) is a genetic testing method that can be used to analyze the DNA sequence of the GPSM2 gene. This test involves sequencing the DNA of an individual to identify any variations or mutations in the GPSM2 gene that may be causing or contributing to the symptoms of Chudley-McCullough syndrome.

By identifying specific genetic changes in the GPSM2 gene, NGS testing can help confirm a diagnosis of Chudley-McCullough syndrome and provide valuable information for genetic counseling, treatment planning, and management of the condition.

SKU: TEST-4050 Category:

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