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MASP1 Gene 3MC Syndrome Type 1 Genetic Test

4,400 د.إ

-21%

The MASP1 gene 3MC Syndrome Type 1 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, aimed at detecting mutations in the MASP1 gene, which are associated with 3MC Syndrome Type 1. This rare, autosomal recessive disorder is characterized by a spectrum of developmental anomalies affecting the craniofacial region, genitalia, umbilicus, and sometimes the cognitive function. The genetic test is crucial for early diagnosis and management of the syndrome, potentially guiding therapeutic interventions and genetic counseling.

The test involves a detailed analysis of the MASP1 gene to identify any genetic mutations that may be indicative of 3MC Syndrome Type 1. Given the complexity and the specialized technology required for this genetic analysis, the cost of the test is 4400 AED. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, this test represents a significant advancement in the field of genetic medicine, offering hope and answers to families affected by this rare condition.

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MASP1 Gene 3MC Syndrome Type 1 Genetic Test

At DNA Labs UAE, we offer the MASP1 Gene 3MC Syndrome Type 1 Genetic Test for individuals who suspect they may have this rare genetic disorder. This test is designed to detect mutations in the MASP1 gene, which is associated with 3MC syndrome type 1.

Test Components and Price

The MASP1 Gene 3MC Syndrome Type 1 Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Method

Once the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology to analyze the MASP1 gene.

Test Type and Doctor

The MASP1 Gene 3MC Syndrome Type 1 Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. It is recommended to consult with a dermatologist for this test.

Test Department and Pre Test Information

The test is conducted in the Genetics department. Prior to the test, it is important to provide the clinical history of the patient who is undergoing the MASP1 Gene 3MC Syndrome Type 1 Genetic Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the MASP1 Gene 3MC Syndrome Type 1 Genetic Test gene.

Test Details

The MASP1 gene is associated with 3MC syndrome type 1, a rare genetic disorder characterized by facial anomalies, intellectual disability, and other developmental abnormalities. NGS genetic testing is used to analyze multiple genes simultaneously, allowing for the detection of genetic variations or mutations associated with 3MC syndrome type 1. This test can be included in NGS genetic testing panels specifically designed to screen for genetic disorders like 3MC syndrome type 1. The panels analyze multiple genes at once, providing a comprehensive assessment of the individual’s genetic makeup and identifying disease-causing mutations.

NGS genetic testing can be performed on a DNA sample obtained from blood or saliva. The results of the test can confirm a diagnosis of 3MC syndrome type 1, guide medical management, and provide information for genetic counseling. It is crucial to consult with a healthcare professional or genetic counselor to determine if NGS genetic testing is appropriate and to understand the potential benefits, limitations, and implications of the test.

Test Name MASP1 Gene 3MC syndrome type 1 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MASP1 Gene 3MC syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MASP1 Gene 3MC syndrome type 1 NGS Genetic DNA Test gene MASP1
Test Details

The MASP1 gene is associated with 3MC syndrome type 1, which is a rare genetic disorder characterized by facial anomalies, intellectual disability, and other developmental abnormalities.

NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. This allows for the detection of genetic variations or mutations that may be associated with a particular disorder, such as 3MC syndrome type 1.

The MASP1 gene can be included in NGS genetic testing panels that are specifically designed to screen for genetic disorders like 3MC syndrome type 1. These panels typically analyze multiple genes at once, providing a comprehensive assessment of the individual’s genetic makeup and identifying any potential disease-causing mutations.

NGS genetic testing can be performed on a DNA sample obtained from a blood or saliva sample. The results of the test can help confirm a diagnosis of 3MC syndrome type 1, guide medical management, and provide information for genetic counseling.

It is important to consult with a healthcare professional or genetic counselor to determine if NGS genetic testing is appropriate and to understand the potential benefits, limitations, and implications of the test.