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FBN1 Gene Stiff Skin Syndrome Genetic Test Cost

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

-21%

The FBN1 Gene Stiff Skin Syndrome Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the FBN1 gene, which are associated with Stiff Skin Syndrome (SSS). Stiff Skin Syndrome is a rare genetic disorder characterized by hard, thick skin that can limit joint mobility and cause discomfort. This condition is primarily caused by mutations in the FBN1 gene, which plays a crucial role in the formation of connective tissue in the body.

The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any abnormalities in the FBN1 gene that might indicate the presence of Stiff Skin Syndrome. This genetic testing is crucial for accurate diagnosis, enabling healthcare professionals to provide appropriate management and treatment plans for affected individuals.

Offered at a cost of 4400 AED, the FBN1 Gene Stiff Skin Syndrome Genetic Test at DNA Labs UAE is an essential tool for individuals experiencing symptoms of SSS or those with a family history of the condition, seeking to understand their genetic health. The test not only aids in the diagnosis but also helps in assessing the risk of passing the condition to future generations, thereby facilitating informed decisions about family planning.

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FBN1 Gene Stiff Skin Syndrome Genetic Test

At DNA Labs UAE, we offer the FBN1 Gene Stiff Skin Syndrome Genetic Test at a cost of AED 4400.0. This test is designed to diagnose Stiff Skin Syndrome (SSS), a rare genetic disorder characterized by thickening and hardening of the skin, limited joint movement, and other related symptoms.

Test Components and Price

The FBN1 Gene Stiff Skin Syndrome Genetic Test costs AED 4400.0. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Method

The report for the FBN1 Gene Stiff Skin Syndrome Genetic Test will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology to analyze the FBN1 gene for any mutations or variations.

Test Type and Doctor

The FBN1 Gene Stiff Skin Syndrome Genetic Test falls under the category of Dysmorphology. It is recommended to consult a Pediatrics doctor for this test.

Test Department and Pre Test Information

The FBN1 Gene Stiff Skin Syndrome Genetic Test is conducted in our Genetics department. Before undergoing the test, it is essential to provide the clinical history of the patient. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected by Stiff Skin Syndrome and the FBN1 gene.

Test Details

The FBN1 gene is associated with Stiff Skin Syndrome (SSS). NGS technology allows for the sequencing of multiple genes simultaneously. In the case of Stiff Skin Syndrome, the FBN1 gene is analyzed for mutations or variations that may be causing the condition. The test involves obtaining a DNA sample from the individual, usually through a blood or saliva sample. The DNA is then extracted and sequenced using NGS technology. The sequencing data is analyzed to identify any mutations or variations in the FBN1 gene that may be responsible for the condition.

This type of genetic testing can confirm a diagnosis of Stiff Skin Syndrome and provide information about the specific genetic mutation involved. It is also useful for carrier testing in individuals with a family history of the condition and for prenatal testing in families at risk of having a child with Stiff Skin Syndrome.

It is crucial to note that genetic testing for Stiff Skin Syndrome should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.

Test Name FBN1 Gene Stiff skin 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 FBN1 Gene Stiff skin syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FBN1 Gene Stiff skin syndrome NGS Genetic DNA Test gene FBN1
Test Details

The FBN1 gene is associated with a condition called Stiff Skin Syndrome (SSS). SSS is a rare genetic disorder characterized by thickening and hardening of the skin, leading to limited joint movement and other related symptoms.

NGS (Next-Generation Sequencing) is a genetic testing technique that allows for the sequencing of multiple genes simultaneously. In the case of Stiff Skin Syndrome, NGS can be used to analyze the FBN1 gene for any mutations or variations that may be causing the condition.

An NGS genetic test for the FBN1 gene in Stiff Skin Syndrome would involve obtaining a DNA sample from the individual, usually through a blood or saliva sample. The DNA is then extracted and sequenced using NGS technology. The sequencing data is analyzed to identify any mutations or variations in the FBN1 gene that may be responsible for the condition.

This type of genetic testing can help confirm a diagnosis of Stiff Skin Syndrome and provide information about the specific genetic mutation involved. It can also be used for carrier testing in individuals with a family history of the condition, and for prenatal testing in families at risk of having a child with Stiff Skin Syndrome.

It is important to note that genetic testing for Stiff Skin Syndrome should be done under the guidance of a healthcare professional or genetic counselor, who can help interpret the results and provide appropriate counseling and support.

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