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KRT71 Gene Hypotrichosis type 13 Genetic Test Cost

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

-21%

The “KRT71 Gene Hypotrichosis Type 13 Genetic Test” is a specialized diagnostic procedure aimed at detecting mutations in the KRT71 gene, which are known to cause Hypotrichosis Type 13. This condition is characterized by a reduced amount of hair on the scalp and other parts of the body, starting from birth or early childhood. The KRT71 gene plays a crucial role in the development and maintenance of hair follicles, and mutations in this gene can lead to abnormalities in hair texture and growth.

Conducted at DNA Labs UAE, this genetic test is a critical tool for individuals exhibiting symptoms of Hypotrichosis Type 13, providing them with a definitive diagnosis. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for any genetic abnormalities associated with the condition.

The cost of the test is set at 4400 AED, reflecting the specialized nature of the testing and the sophisticated technology employed in the analysis. This test not only facilitates the accurate diagnosis of Hypotrichosis Type 13 but also enables affected individuals and their families to understand the genetic basis of the condition, paving the way for appropriate management and treatment strategies.

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KRT71 Gene Hypotrichosis type 13 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 KRT71 Gene Hypotrichosis type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KRT71 Gene Hypotrichosis type 13 NGS Genetic DNA Test gene KRT71

Test Details

The KRT71 gene is associated with a condition called Hypotrichosis type 13, which is a rare form of hair loss. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze an individual’s DNA to identify any genetic variations or mutations that may be causing the condition. NGS genetic testing involves sequencing the entire KRT71 gene to identify any changes in the DNA sequence that may be contributing to the development of Hypotrichosis type 13. This can help in confirming a diagnosis, determining the specific genetic cause of the condition, and providing information about the inheritance pattern. By identifying the specific genetic mutation, NGS genetic testing can also be used for carrier testing in family members, genetic counseling, and potentially for prenatal testing in future pregnancies. It is important to note that genetic testing for Hypotrichosis type 13 is typically done in specialized laboratories and should be conducted under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and management options.

Test Name KRT71 Gene Hypotrichosis type 13 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 KRT71 Gene Hypotrichosis type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KRT71 Gene Hypotrichosis type 13 NGS Genetic DNA Test gene KRT71
Test Details

The KRT71 gene is associated with a condition called Hypotrichosis type 13, which is a rare form of hair loss. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze an individual’s DNA to identify any genetic variations or mutations that may be causing the condition.

NGS genetic testing involves sequencing the entire KRT71 gene to identify any changes in the DNA sequence that may be contributing to the development of Hypotrichosis type 13. This can help in confirming a diagnosis, determining the specific genetic cause of the condition, and providing information about the inheritance pattern.

By identifying the specific genetic mutation, NGS genetic testing can also be used for carrier testing in family members, genetic counseling, and potentially for prenatal testing in future pregnancies.

It is important to note that genetic testing for Hypotrichosis type 13 is typically done in specialized laboratories and should be conducted under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and management options.

SKU: TEST-3037 Category:

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