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ALDH18A1 Gene Cutis Laxa Type 3A Autosomal Recessive Genetic Test

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

-21%

The ALDH18A1 gene plays a crucial role in the biosynthesis of proline, an amino acid important for the proper structure and function of proteins. Mutations in this gene can lead to Cutis Laxa Type 3A, a rare genetic disorder characterized by loose, sagging skin and a variety of systemic symptoms including joint laxity, developmental delays, and, in some cases, neurological issues. This autosomal recessive condition means that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

DNA Labs UAE offers a specialized genetic test to identify mutations in the ALDH18A1 gene, aiding in the diagnosis of Cutis Laxa Type 3A. This test is crucial for families seeking answers to unexplained symptoms related to skin elasticity and systemic involvement that may suggest this rare condition. The test cost is set at 4400 AED, reflecting the comprehensive analysis and the specialized expertise required to interpret the results accurately.

Undergoing this test can be an important step for affected individuals and their families to understand the genetic underpinnings of their condition, paving the way for tailored management and support strategies.

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ALDH18A1 Gene Cutis Laxa Type 3A Autosomal Recessive Genetic Test

At DNA Labs UAE, we offer the ALDH18A1 Gene Cutis Laxa Type 3A Autosomal Recessive Genetic Test to help diagnose and understand this genetic disorder. This test is designed to identify mutations in the ALDH18A1 gene that are associated with Cutis Laxa Type 3A.

Test Components

  • Price: 4400.0 AED
  • Sample Condition: Blood
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Osteology Dermatology Immunology Disorders

Doctor and Test Department

This test is performed by a Dermatologist in our Genetics Test Department.

Pre Test Information

Prior to the ALDH18A1 Gene Cutis Laxa Type 3A Autosomal Recessive Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by this genetic disorder.

About the ALDH18A1 Gene and Cutis Laxa Type 3A

The ALDH18A1 gene is associated with Cutis Laxa Type 3A, a genetic disorder. This disorder is inherited in an autosomal recessive manner, meaning that both copies of the mutated gene must be inherited from each parent for the condition to develop.

NGS Technology and Genetic Testing

Next-Generation Sequencing (NGS) genetic testing is used to analyze multiple genes simultaneously, allowing for the detection of genetic mutations or variations associated with specific disorders. In the case of Cutis Laxa Type 3A, NGS genetic testing can identify mutations in the ALDH18A1 gene that may be responsible for the condition.

By analyzing the DNA sequence of the ALDH18A1 gene, NGS genetic testing provides information about any genetic variations or mutations that may be present. This information is valuable for confirming a diagnosis of Cutis Laxa Type 3A, as well as for genetic counseling and family planning purposes.

Please note that NGS genetic testing may not be available in all healthcare settings, and the specific details of the test may vary depending on the laboratory or testing facility. We recommend consulting with a healthcare professional or genetic counselor for more information about the availability and specifics of the ALDH18A1 Gene Cutis Laxa Type 3A Autosomal Recessive NGS Genetic Test.

Test Name ALDH18A1 Gene Cutis laxa type 3A autosomal recessive Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
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 ALDH18A1 Gene Cutis laxa type 3A, autosomal recessive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ALDH18A1 Gene Cutis laxa type 3A, autosomal recessive NGS Genetic DNA Test gene ALDH18A1
Test Details

The ALDH18A1 gene is associated with a genetic disorder called Cutis laxa type 3A. This disorder is inherited in an autosomal recessive manner, meaning that an affected individual must inherit two copies of the mutated gene (one from each parent) in order to develop the condition.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the detection of genetic mutations or variations that may be associated with a particular disorder. In the case of Cutis laxa type 3A, NGS genetic testing can be used to identify mutations in the ALDH18A1 gene that may be responsible for the condition.

By analyzing the DNA sequence of the ALDH18A1 gene, NGS genetic testing can provide information about any genetic variations or mutations that may be present. This information can help in confirming a diagnosis of Cutis laxa type 3A and can also be useful for genetic counseling and family planning purposes.

It is important to note that NGS genetic testing may not be available in all healthcare settings, and the specific details of the test may vary depending on the laboratory or testing facility. It is recommended to consult with a healthcare professional or a genetic counselor for more information about the availability and specifics of the ALDH18A1 gene Cutis laxa type 3A autosomal recessive NGS genetic test.

SKU: TEST-2912 Category:

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