KRT14 Gene Epidermolysis bullosa simplex Weber-Cockayne type Genetic Test sale cost 4400 AED
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KRT14 Gene Epidermolysis bullosa simplex Weber-Cockayne type Genetic Test Cost

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

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The KRT14 Gene Epidermolysis Bullosa Simplex Weber-Cockayne Type Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE. This test is designed to identify mutations in the KRT14 gene, which are associated with the development of Epidermolysis Bullosa Simplex (EBS), specifically the Weber-Cockayne type. EBS is a group of genetic skin disorders that cause the skin to be very fragile and to blister easily. The Weber-Cockayne type is typically the mildest form of EBS, mainly affecting the palms of the hands and soles of the feet.

The genetic test involves analyzing the patient’s DNA to search for specific mutations in the KRT14 gene that are known to cause the disorder. This is crucial for accurate diagnosis, enabling personalized treatment plans and management strategies for affected individuals. It also provides valuable information for family planning and genetic counseling for families with a history of the condition.

The cost of the KRT14 Gene Epidermolysis Bullosa Simplex Weber-Cockayne Type Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the presence of the genetic mutations associated with the condition. By opting for this test, patients and their families can gain insights into their genetic makeup, paving the way for informed medical and personal decisions.

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KRT14 Gene Epidermolysis bullosa simplex Weber-Cockayne type Genetic Test

Welcome to the DNA Labs UAE blog! Today, we will be discussing the KRT14 Gene Epidermolysis bullosa simplex Weber-Cockayne type Genetic Test. This test is specifically designed to diagnose and identify the KRT14 gene associated with a condition called epidermolysis bullosa simplex (EBS), specifically the Weber-Cockayne type.

Test Details

Epidermolysis bullosa simplex (EBS) is a rare genetic disorder characterized by blistering of the skin and mucous membranes. It is caused by mutations in genes that provide instructions for making keratins, which are proteins that help maintain the structure and integrity of the skin. The KRT14 gene is one of the genes associated with EBS.

Our KRT14 Gene Epidermolysis bullosa simplex Weber-Cockayne type Genetic Test utilizes Next-Generation Sequencing (NGS) technology. NGS genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of EBS, NGS can be used to identify mutations or variations in the KRT14 gene that may be responsible for the disease.

To perform the test, we require a DNA sample, which can be obtained through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to analyze the entire coding region of the KRT14 gene, as well as other relevant genes associated with EBS. The test aims to identify any disease-causing mutations or variations in these genes.

Test Components and Price

The cost of the KRT14 Gene Epidermolysis bullosa simplex Weber-Cockayne type Genetic Test is 4400.0 AED. The test can be performed using a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Method

The report for the KRT14 Gene Epidermolysis bullosa simplex Weber-Cockayne type Genetic Test will be delivered within 3 to 4 weeks. The test is conducted using NGS technology.

Test Type and Doctor

The KRT14 Gene Epidermolysis bullosa simplex Weber-Cockayne type Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. The test is typically ordered by dermatologists and is performed in our Genetics department.

Pre Test Information

Prior to undergoing the KRT14 Gene Epidermolysis bullosa simplex Weber-Cockayne type Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected with KRT14 Gene Epidermolysis bullosa simplex, Weber-Cockayne type NGS Genetic DNA Test gene KRT14.

Conclusion

NGS genetic testing for the KRT14 gene associated with Epidermolysis bullosa simplex Weber-Cockayne type is a valuable tool for confirming a diagnosis, understanding the genetic cause of the disease, and guiding treatment decisions. It can also be useful for genetic counseling and family planning purposes. It is important to consult qualified healthcare professionals specializing in genetics for the performance and interpretation of genetic testing.

Test Name KRT14 Gene Epidermolysis bullosa simplex Weber-Cockayne type 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 KRT14 Gene Epidermolysis bullosa simplex, Weber-Cockayne type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KRT14 Gene Epidermolysis bullosa simplex, Weber-Cockayne type NGS Genetic DNA Test gene KRT14
Test Details

The KRT14 gene is associated with a condition called epidermolysis bullosa simplex (EBS), specifically the Weber-Cockayne type. EBS is a rare genetic disorder characterized by blistering of the skin and mucous membranes. It is caused by mutations in genes that provide instructions for making keratins, which are proteins that help maintain the structure and integrity of the skin.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of EBS, NGS can be used to identify mutations or variations in the KRT14 gene that may be responsible for the disease.

The NGS genetic test for KRT14 gene EBS involves obtaining a DNA sample, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to analyze the entire coding region of the KRT14 gene, as well as other relevant genes associated with EBS. The test aims to identify any disease-causing mutations or variations in these genes.

NGS genetic testing for KRT14 gene EBS can help confirm a diagnosis, provide information about the specific genetic cause of the disease, and inform treatment decisions. It can also be useful for genetic counseling and family planning purposes. It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals who specialize in genetics.

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