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FBLN5 Gene Cutis Laxa Type 2 Autosomal Dominant Genetic Test Cost

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

-21%

The FBLN5 gene is associated with a rare condition known as Cutis Laxa Type 2, which is an autosomal dominant disorder. This condition is characterized by the appearance of loose, sagging skin and can also affect internal organs, leading to a variety of health issues. The FBLN5 gene plays a crucial role in the formation and maintenance of elastic fibers in connective tissue, and mutations in this gene can disrupt these processes, leading to the symptoms observed in Cutis Laxa Type 2.

To diagnose this condition, a genetic test targeting the FBLN5 gene can be conducted. DNA Labs UAE offers this specific genetic test, providing a crucial tool for individuals and families seeking answers about this rare disorder. The test is priced at 4400 AED and involves collecting a DNA sample from the patient, usually through a blood draw or a cheek swab. The sample is then analyzed in the laboratory to identify any mutations in the FBLN5 gene that may be indicative of Cutis Laxa Type 2.

This genetic test is not only important for diagnosing affected individuals but also for understanding the risk of passing the condition on to future generations. With the results, families can make informed decisions regarding health management, potential treatments, and genetic counseling. DNA Labs UAE ensures confidentiality and accuracy in the testing process, providing a crucial service for those impacted by this rare genetic disorder.

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FBLN5 Gene Cutis Laxa Type 2 Autosomal Dominant Genetic Test

Test Name: FBLN5 Gene Cutis Laxa Type 2 Autosomal Dominant Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 FBLN5 Gene Cutis Laxa Type 2, Autosomal Dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FBLN5 Gene Cutis Laxa Type 2, Autosomal Dominant NGS Genetic DNA Test gene FBLN5.

Test Details

The FBLN5 gene is associated with a condition called cutis laxa type 2, which is an autosomal dominant disorder. Cutis laxa is a connective tissue disorder characterized by loose, sagging skin and other connective tissue abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the context of cutis laxa type 2, NGS genetic testing can be used to identify mutations or variations in the FBLN5 gene that may be responsible for the condition.

This type of genetic testing involves sequencing the DNA of an individual to detect any changes or mutations in the FBLN5 gene. It can provide valuable information about the genetic cause of cutis laxa type 2, which can aid in diagnosis, genetic counseling, and potentially guide treatment options.

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.

Test Name FBLN5 Gene Cutis laxa type 2 autosomal dominant 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 FBLN5 Gene Cutis laxa type 2, autosomal dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FBLN5 Gene Cutis laxa type 2, autosomal dominant NGS Genetic DNA Test gene FBLN5
Test Details

The FBLN5 gene is associated with a condition called cutis laxa type 2, which is an autosomal dominant disorder. Cutis laxa is a connective tissue disorder characterized by loose, sagging skin and other connective tissue abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the context of cutis laxa type 2, NGS genetic testing can be used to identify mutations or variations in the FBLN5 gene that may be responsible for the condition.

This type of genetic testing involves sequencing the DNA of an individual to detect any changes or mutations in the FBLN5 gene. It can provide valuable information about the genetic cause of cutis laxa type 2, which can aid in diagnosis, genetic counseling, and potentially guide treatment options.

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.

SKU: TEST-2909 Category:

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