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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 tool used to identify mutations in the FBN1 gene, which are associated with Stiff Skin Syndrome (SSS). This condition is a rare genetic disorder characterized by hard, thick skin that can limit mobility and cause discomfort. The test is crucial for early diagnosis and management of the condition, enabling healthcare professionals to tailor treatment plans to the specific needs of the patient.

Conducted at DNA Labs UAE, a leading facility in genetic testing, the test offers a comprehensive analysis of the FBN1 gene. With state-of-the-art technology and a team of expert geneticists, DNA Labs UAE ensures accurate and reliable results. The cost of the test is 4400 AED, an investment in obtaining crucial genetic information that can significantly impact the patient’s quality of life and management of Stiff Skin Syndrome.

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FBN1 Gene Stiff skin syndrome Genetic Test – Cost, Symptoms, Diagnosis

Welcome to DNA Labs UAE, your trusted genetic lab for all your testing needs. Today, we will be discussing the FBN1 Gene Stiff skin syndrome Genetic Test, its cost, symptoms, and diagnosis process.

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: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the FBN1 Gene Stiff skin syndrome Genetic Test, it is important to provide the clinical history of the patient. A Genetic Counselling session will be conducted 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 rare genetic disorder called Stiff Skin Syndrome (SSS). This condition is characterized by thickened and hardened skin, joint contractures, and limited joint movement. The cause of SSS is mutations in the FBN1 gene, which produces the fibrillin-1 protein.

The FBN1 Gene Stiff skin syndrome Genetic Test utilizes next-generation sequencing (NGS) technology to analyze the FBN1 gene and identify any mutations or variations present. This test confirms the diagnosis of Stiff Skin Syndrome and determines the specific genetic variant responsible for the condition.

NGS technology allows for the simultaneous analysis of multiple genes, making it a powerful tool for diagnosing genetic disorders. In the case of Stiff Skin Syndrome, an NGS panel may include other genes associated with similar connective tissue disorders to rule out other possible diagnoses.

Genetic testing provides crucial information for individuals and families affected by Stiff Skin Syndrome. It helps in understanding the cause of the condition, predicting its progression, and informing treatment and management strategies. Additionally, genetic testing aids in family planning decisions and genetic counseling for at-risk individuals.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our team of dermatologists and geneticists specialize in diagnosing and managing genetic disorders. If you suspect Stiff Skin Syndrome or have a family history of the condition, we recommend considering the FBN1 Gene Stiff skin syndrome Genetic Test. Contact us today to schedule an appointment and take control of your genetic health.

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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
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 thickened and hardened skin, joint contractures, and limited joint movement. It is caused by mutations in the FBN1 gene, which provides instructions for producing a protein called fibrillin-1.

A next-generation sequencing (NGS) genetic test can be used to analyze the FBN1 gene and identify any mutations or variations that may be present. This test can help in confirming a diagnosis of Stiff Skin Syndrome and determining the specific genetic variant responsible for the condition.

NGS technology allows for the simultaneous analysis of multiple genes, making it a powerful tool for diagnosing genetic disorders. In the case of Stiff Skin Syndrome, an NGS panel may include other genes associated with similar connective tissue disorders to rule out other possible diagnoses.

Genetic testing can provide important information for individuals and families affected by Stiff Skin Syndrome. It can help in understanding the cause of the condition, predicting its progression, and informing treatment and management strategies. Additionally, genetic testing can aid in family planning decisions and genetic counseling for at-risk individuals.