ELN Gene Cutis Laxa Autosomal Dominant Genetic Test
Test Name: ELN Gene Cutis Laxa Autosomal Dominant Genetic Test
Components: DNA Labs UAE offers the ELN Gene Cutis Laxa Autosomal Dominant Genetic Test at a price of 4400.0 AED.
Sample Condition: The test requires a blood or extracted DNA sample, or one drop of blood on an FTA Card.
Report Delivery: The test results will be delivered within 3 to 4 weeks.
Method: The ELN Gene Cutis Laxa Autosomal Dominant Genetic Test utilizes NGS (Next-Generation Sequencing) technology.
Test Type: The test is specifically designed to detect osteology, dermatology, and immunology disorders.
Doctor: A dermatologist will oversee the ELN Gene Cutis Laxa Autosomal Dominant Genetic Test.
Test Department: The test falls under the Genetics department.
Pre Test Information: Prior to the test, a clinical history of the patient will be collected. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the ELN Gene Cutis Laxa Autosomal Dominant Genetic Test gene ELN.
Test Details:
The ELN Gene Cutis Laxa Autosomal Dominant Genetic Test is designed to diagnose a genetic disorder that affects the connective tissue, resulting in loose and sagging skin. This disorder is caused by mutations in the ELN gene, which provides instructions for the production of elastin, a vital component of the extracellular matrix responsible for tissue elasticity and strength.
An autosomal dominant inheritance pattern means that only one copy of the mutated gene is required from either parent for the disorder to develop. Consequently, each child of an affected individual has a 50% chance of inheriting the mutation and developing Cutis Laxa.
NGS (Next-Generation Sequencing) genetic testing is employed to analyze multiple genes simultaneously and identify genetic mutations associated with specific disorders. In the case of the ELN Gene Cutis Laxa, NGS is used to detect mutations in the ELN gene. This involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the DNA to identify any variations or mutations in the ELN gene.
This test aids in confirming a diagnosis of Cutis Laxa and provides information about the specific mutation causing the disorder. It is particularly helpful for individuals displaying symptoms of Cutis Laxa or those with a family history of the disorder. A definitive diagnosis obtained through genetic testing can guide treatment decisions and assist in genetic counseling for family planning purposes.
However, it is crucial to consult with a healthcare professional or genetic counselor before undergoing any genetic testing. This will ensure a comprehensive understanding of the benefits, limitations, and potential implications of the test results.
Test Name | ELN Gene Cutis laxa autosomal dominant Genetic Test |
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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 ELN Gene Cutis laxa, autosomal dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ELN Gene Cutis laxa, autosomal dominant NGS Genetic DNA Test gene ELN |
Test Details |
ELN gene Cutis laxa is a genetic disorder that affects the connective tissue, leading to loose and sagging skin. It is caused by mutations in the ELN gene, which provides instructions for making a protein called elastin. Elastin is an important component of the extracellular matrix, which gives tissues their elasticity and strength. An autosomal dominant inheritance pattern means that a person only needs to inherit one copy of the mutated gene from either parent to develop the disorder. This means that each child of an affected individual has a 50% chance of inheriting the mutation and developing Cutis laxa. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic mutations associated with a particular disorder. In the case of ELN gene Cutis laxa, NGS can be used to detect mutations in the ELN gene. NGS genetic testing involves obtaining a DNA sample, usually through a blood or saliva sample, and sequencing the DNA to identify any variations or mutations in the ELN gene. This can help in confirming a diagnosis of Cutis laxa and provide information about the specific mutation causing the disorder. Genetic testing can be helpful for individuals who have symptoms of Cutis laxa or have a family history of the disorder. It can provide a definitive diagnosis, guide treatment decisions, and help in genetic counseling for family planning purposes. However, it is important to consult with a healthcare professional or genetic counselor before undergoing any genetic testing to understand the benefits, limitations, and potential implications of the test results. |