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IFT172 Gene Short-Rib Thoracic Dysplasia Type 10 with or Without Polydactyly Genetic Test Cost

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

-21%

The IFT172 gene plays a crucial role in the development of bones and other tissues within the body. Mutations in this gene are associated with Short-Rib Thoracic Dysplasia Type 10 with or without Polydactyly (SRTD10), a rare genetic disorder characterized by constricted thoracic cage, short ribs, shortened bones in the arms and legs, and in some cases, extra fingers or toes (polydactyly). This condition is part of a group of diseases known as ciliopathies, which are caused by dysfunction of cilia, microscopic hair-like structures that play a critical role in cellular signaling and organ development.

DNA Labs UAE offers a genetic test specifically designed to identify mutations in the IFT172 gene, providing crucial information for the diagnosis of Short-Rib Thoracic Dysplasia Type 10. This test is particularly valuable for families with a history of the condition or where prenatal diagnosis is considered. The cost of the test is 4400 AED and involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of genetic mutations associated with the disorder.

By confirming a diagnosis, this genetic test enables healthcare providers to offer appropriate clinical management and counseling for affected individuals and their families. It also aids in understanding the risk of recurrence in future pregnancies, allowing for informed decision-making. DNA Labs UAE, with its state-of-the-art facilities and expert team, ensures accurate and reliable testing results, contributing to the effective diagnosis and understanding of Short-Rib Thoracic Dysplasia Type 10.

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Genetic Lab Blog: IFT172 Gene Short-rib thoracic dysplasia type 10 with or without polydactyly Genetic Test

Genetic testing plays a crucial role in diagnosing and understanding rare genetic disorders. In this blog, we will discuss the IFT172 Gene Short-rib thoracic dysplasia type 10 with or without polydactyly Genetic Test offered by DNA Labs UAE.

Test Details

The IFT172 gene is associated with a rare genetic disorder known as short-rib thoracic dysplasia type 10 with or without polydactyly. This disorder primarily affects the skeletal system, particularly the ribs and long bones. It is also characterized by the presence of extra fingers or toes, a condition called polydactyly.

The IFT172 Gene Short-rib thoracic dysplasia type 10 with or without polydactyly Genetic Test offered by DNA Labs UAE utilizes NGS (Next-Generation Sequencing) technology. This advanced method allows for the analysis of the IFT172 gene to identify any mutations or variations that may be present.

By sequencing the DNA in the IFT172 gene, this genetic test can help confirm a diagnosis of short-rib thoracic dysplasia type 10 with or without polydactyly. Additionally, it provides valuable information about the specific mutation(s) present, which can be useful for genetic counseling and family planning.

Test Components and Price

The cost of the IFT172 Gene Short-rib thoracic dysplasia type 10 with or without polydactyly Genetic Test is AED 4400.0. The test requires a sample condition of blood, extracted DNA, or one drop of blood on an FTA Card.

Report Delivery and Method

After the sample is collected, the report delivery time for this genetic test is approximately 3 to 4 weeks. The method used for the test is NGS (Next-Generation Sequencing) technology.

Test Type, Doctor, and Test Department

The IFT172 Gene Short-rib thoracic dysplasia type 10 with or without polydactyly Genetic Test falls under the category of dysmorphology tests. It is recommended to consult with a pediatrician for this specific test. The test department responsible for conducting this genetic test is the Genetics department.

Pre Test Information

Prior to undergoing the IFT172 Gene Short-rib thoracic dysplasia type 10 with or without polydactyly NGS Genetic DNA Test, it is essential to provide the clinical history of the patient. This includes information about the patient’s symptoms and any relevant medical history.

A genetic counseling session is also recommended to draw a pedigree chart of family members affected by the IFT172 Gene Short-rib thoracic dysplasia type 10 with or without polydactyly NGS Genetic DNA Test gene IFT172. This session helps in understanding the inheritance pattern and identifying potential carriers of the disorder.

It is important to note that genetic testing should always be conducted by a qualified healthcare professional or genetic counselor. They possess the expertise to interpret the test results accurately and provide appropriate guidance and support.

Test Name IFT172 Gene Short-rib thoracic dysplasia type 10 with or without polydactyly 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 IFT172 Gene Short-rib thoracic dysplasia type 10 with or without polydactyly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with IFT172 Gene Short-rib thoracic dysplasia type 10 with or without polydactyly NGS Genetic DNA Test gene IFT172
Test Details

IFT172 gene is associated with a rare genetic disorder called short-rib thoracic dysplasia type 10 with or without polydactyly. This disorder is characterized by skeletal abnormalities, particularly affecting the ribs and long bones, as well as extra fingers or toes (polydactyly).

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the IFT172 gene for any mutations or variations that may be present. This test involves sequencing the DNA in the gene to identify any changes that may be causing the disorder.

By identifying mutations in the IFT172 gene, NGS genetic testing can help confirm a diagnosis of short-rib thoracic dysplasia type 10 with or without polydactyly. It can also provide information about the specific mutation(s) present, which can be useful for genetic counseling and family planning.

It is important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

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