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POMP Gene Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Genetic Test Cost

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

-21%

The “POMP Gene Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Genetic Test” is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the POMP gene. These mutations are associated with a rare genetic disorder characterized by a combination of skin conditions, including keratosis linearis, ichthyosis congenita, and sclerosing keratoderma. The test aims to provide crucial genetic information that can help in the diagnosis and management of these conditions.

The procedure involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of specific genetic alterations in the POMP gene. This gene plays a significant role in skin development and health, and mutations can lead to the aforementioned complex skin disorders.

The cost of the test is 4400 AED, reflecting the specialized nature of the genetic analysis and the valuable insights it offers for affected individuals and their families. By identifying the genetic underpinnings of these conditions, healthcare providers can better understand the disease mechanism, predict its progression, and tailor treatment plans to manage symptoms effectively. DNA Labs UAE, with its state-of-the-art facilities and expertise in genetic diagnostics, ensures high-quality testing and reliable results for patients seeking answers to complex genetic questions.

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POMP Gene Keratosis linearis with ichthyosis congenita and sclerosing keratoderma Genetic Test

Welcome to DNA Labs UAE’s blog on the POMP Gene Keratosis linearis with ichthyosis congenita and sclerosing keratoderma Genetic Test. In this blog, we will discuss the symptoms, diagnosis, and cost of this genetic test.

Test Name

POMP Gene Keratosis linearis with ichthyosis congenita and sclerosing keratoderma Genetic Test

Components and Price

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 POMP Gene Keratosis linearis with ichthyosis congenita and sclerosing keratoderma NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with POMP Gene Keratosis linearis with ichthyosis congenita and sclerosing keratoderma NGS Genetic DNA Test gene POMP.

Test Details

POMP gene mutations have been associated with a rare genetic disorder known as keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK). KLICK is characterized by dry, scaly skin (ichthyosis), thickening of the skin on the palms and soles (sclerosing keratoderma), and linear ridges on the palms and soles (keratosis linearis).

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the POMP gene and identify mutations or variations that may be responsible for KLICK. NGS is a high-throughput sequencing technology that allows for the simultaneous sequencing of multiple genes or the entire genome. It can provide a comprehensive analysis of the POMP gene, enabling the identification of disease-causing mutations or variants.

Genetic testing for KLICK can be helpful in confirming a diagnosis, providing genetic counseling, and guiding treatment decisions. It can also assist in family planning and prenatal testing for individuals at risk of having a child with KLICK.

It is important to note that genetic testing for KLICK should be conducted by a qualified healthcare professional or genetic counselor, who can interpret the results and provide appropriate guidance and support.

Test Name POMP Gene Keratosis linearis with ichthyosis congenita and sclerosing keratoderma 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 POMP Gene Keratosis linearis with ichthyosis congenita and sclerosing keratoderma NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with POMP Gene Keratosis linearis with ichthyosis congenita and sclerosing keratoderma NGS Genetic DNA Test gene POMP
Test Details

POMP gene mutations have been associated with a rare genetic disorder known as keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK). KLICK is characterized by dry, scaly skin (ichthyosis), thickening of the skin on the palms and soles (sclerosing keratoderma), and linear ridges on the palms and soles (keratosis linearis).

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the POMP gene and identify mutations or variations that may be responsible for KLICK. NGS is a high-throughput sequencing technology that allows for the simultaneous sequencing of multiple genes or the entire genome. It can provide a comprehensive analysis of the POMP gene, enabling the identification of disease-causing mutations or variants.

Genetic testing for KLICK can be helpful in confirming a diagnosis, providing genetic counseling, and guiding treatment decisions. It can also assist in family planning and prenatal testing for individuals at risk of having a child with KLICK.

It is important to note that genetic testing for KLICK should be conducted by a qualified healthcare professional or genetic counselor, who can interpret the results and provide appropriate guidance and support.