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FAM20C Gene Raine Syndrome Genetic Test Cost

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

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The FAM20C gene is associated with Raine Syndrome, a rare genetic disorder characterized by bone abnormalities, craniofacial anomalies, and various other clinical features. Raine Syndrome is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected by the condition.

The genetic test for Raine Syndrome focuses on identifying mutations in the FAM20C gene, which plays a crucial role in bone mineralization and development. This test is essential for the accurate diagnosis of the syndrome, allowing for early intervention and management of symptoms. It can also provide vital information for family planning and genetic counseling for families with a history of the condition.

At DNA Labs UAE, the FAM20C gene test for Raine Syndrome is offered at a cost of 4400 AED. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations in the FAM20C gene. The process is conducted by experienced geneticists and laboratory technicians, ensuring accurate and reliable results. This test is a valuable resource for families seeking answers about this rare genetic disorder and its implications for their health and future.

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FAM20C Gene Raine syndrome Genetic Test

At DNA Labs UAE, we offer the FAM20C Gene Raine syndrome Genetic Test for individuals suspected of having Raine syndrome. Raine syndrome is a rare genetic disorder characterized by craniofacial abnormalities, skeletal abnormalities, and severe intellectual disability.

Test Components and Price

The FAM20C Gene Raine syndrome 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

The test results will be delivered within 3 to 4 weeks after sample submission.

Method

The FAM20C Gene Raine syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology. This advanced sequencing method allows for the rapid analysis of multiple genes simultaneously.

Test Type

The FAM20C Gene Raine syndrome Genetic Test falls under the categories of Osteology, Dermatology, and Immunology Disorders.

Referring Doctor and Test Department

The test is typically ordered by a Dermatologist and is performed in our Genetics department.

Pre Test Information

Prior to undergoing the FAM20C Gene Raine syndrome NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected by the disorder.

Test Details

The FAM20C gene is associated with Raine syndrome. This genetic disorder presents with various symptoms, including craniofacial abnormalities, skeletal abnormalities, and severe intellectual disability.

NGS genetic testing allows for a comprehensive analysis of the FAM20C gene. By identifying mutations or variations in this gene, a more accurate diagnosis of Raine syndrome can be made. This information is valuable for genetic counseling and the development of appropriate treatment and management plans for affected individuals.

Test Name FAM20C Gene Raine 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FAM20C Gene Raine syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FAM20C Gene Raine syndrome NGS Genetic DNA Test gene FAM20C
Test Details

The FAM20C gene is associated with a rare genetic disorder called Raine syndrome. Raine syndrome is characterized by a variety of symptoms including craniofacial abnormalities, skeletal abnormalities, and severe intellectual disability.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to rapidly analyze multiple genes simultaneously. In the context of Raine syndrome, NGS genetic testing can be used to identify mutations or variations in the FAM20C gene that may be responsible for the disorder.

NGS genetic testing can provide a comprehensive analysis of the FAM20C gene, allowing for a more accurate diagnosis of Raine syndrome. This information can be useful for genetic counseling, as well as for developing appropriate treatment and management plans for individuals with the disorder.

SKU: TEST-3236 Category:

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