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USB1 Gene Poikiloderma with Neutropenia Genetic Test

4,400 د.إ

-21%

The USB1 Gene Poikiloderma with Neutropenia Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the USB1 gene, which are known to cause Poikiloderma with Neutropenia (PN). PN is a rare genetic condition characterized by a specific skin rash (poikiloderma), nail abnormalities, and a predisposition to developing neutropenia, a condition involving an abnormally low count of neutrophils, a type of white blood cell crucial for fighting off infections.

This test is particularly important for individuals showing symptoms of PN or those with a family history of the condition, as early and accurate diagnosis can significantly improve management strategies and outcomes. By analyzing the patient’s DNA, the test can confirm the presence of the genetic mutations associated with PN, providing essential information for genetic counseling and guiding treatment decisions.

The cost of the USB1 Gene Poikiloderma with Neutropenia Genetic Test at DNA Labs UAE is set at 4400 AED. Given the complexity of the condition and the specialized nature of the test, this price reflects the intricate processes involved in genetic analysis and the expert interpretation of results. Patients considering this test are advised to consult with their healthcare provider to understand its benefits and implications fully.

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USB1 Gene Poikiloderma with neutropenia Genetic Test

Welcome to DNA Labs UAE, a leading genetic laboratory offering comprehensive genetic testing services. In this blog, we will provide detailed information about the USB1 Gene Poikiloderma with neutropenia Genetic Test, including its components, cost, symptoms, diagnosis, and more.

Test Name: USB1 Gene Poikiloderma with neutropenia 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

Before undergoing the USB1 Gene Poikiloderma with neutropenia Genetic Test, it is important to provide the clinical history of the patient. A Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with USB1 Gene Poikiloderma with neutropenia NGS Genetic DNA Test gene USB1.

Test Details

The USB1 gene, also known as Usher syndrome type 1B gene, is associated with a rare genetic disorder called poikiloderma with neutropenia. This disorder is characterized by a combination of skin abnormalities (poikiloderma) and low levels of neutrophils in the blood (neutropenia).

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes, including the USB1 gene. This test involves sequencing the DNA of an individual to identify any genetic variations or mutations that may be responsible for the development of poikiloderma with neutropenia.

By identifying the specific genetic mutation in the USB1 gene, NGS genetic testing can help confirm a diagnosis of poikiloderma with neutropenia and provide information about the inheritance pattern of the disorder. This information can be useful for genetic counseling, family planning, and potentially guiding treatment options in the future.

It is important to note that while NGS genetic testing can provide valuable information, it is not a cure for poikiloderma with neutropenia. Treatment for this disorder is typically focused on managing the symptoms and complications associated with the condition.

For more information about the USB1 Gene Poikiloderma with neutropenia Genetic Test or to schedule an appointment, please contact DNA Labs UAE.

Test Name USB1 Gene Poikiloderma with neutropenia 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 USB1 Gene Poikiloderma with neutropenia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with USB1 Gene Poikiloderma with neutropenia NGS Genetic DNA Test gene USB1
Test Details

USB1 gene, also known as Usher syndrome type 1B gene, is associated with a rare genetic disorder called poikiloderma with neutropenia. This disorder is characterized by a combination of skin abnormalities (poikiloderma) and low levels of neutrophils in the blood (neutropenia).

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes, including the USB1 gene. This test involves sequencing the DNA of an individual to identify any genetic variations or mutations that may be responsible for the development of poikiloderma with neutropenia.

By identifying the specific genetic mutation in the USB1 gene, NGS genetic testing can help confirm a diagnosis of poikiloderma with neutropenia and provide information about the inheritance pattern of the disorder. This information can be useful for genetic counseling, family planning, and potentially guiding treatment options in the future.

It is important to note that while NGS genetic testing can provide valuable information, it is not a cure for poikiloderma with neutropenia. Treatment for this disorder is typically focused on managing the symptoms and complications associated with the condition.

SKU: TEST-3218 Category:

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