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DSP Gene Keratosis Palmoplantaris Striata Type 2 Genetic Test Cost

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

-21%

The DSP Gene Keratosis Palmoplantaris Striata Type 2 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the DSP gene that are associated with Keratosis Palmoplantaris Striata Type 2. This condition, also known as Striate Palmoplantar Keratoderma Type 2, is a rare genetic disorder characterized by the development of thickened skin on the palms of the hands and the soles of the feet, often presenting in a striated pattern. The test is crucial for individuals who exhibit symptoms of the condition or have a family history of the disorder, as it can confirm the diagnosis and inform potential treatment strategies.

Performed in a state-of-the-art laboratory setting, the test involves analyzing the patient’s DNA sample, typically obtained through a blood draw or cheek swab, to detect specific mutations in the DSP gene that are indicative of the disorder. The DSP gene plays a significant role in the development and function of the skin and its structures, making mutations in this gene a key factor in the development of Keratosis Palmoplantaris Striata Type 2.

The cost of the DSP Gene Keratosis Palmoplantaris Striata Type 2 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, including the advanced genetic analysis required to identify the relevant DSP gene mutations. Patients considering this test are advised to consult with a healthcare professional or genetic counselor to discuss the implications of the results and any subsequent steps that should be taken in light of a positive diagnosis.

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DSP Gene Keratosis palmoplantaris striata type 2 Genetic Test

Welcome to DNA Labs UAE, where we offer the DSP Gene Keratosis palmoplantaris striata type 2 Genetic Test. This genetic test uses Next-Generation Sequencing (NGS) technology to analyze the DSP gene for mutations associated with Keratosis palmoplantaris striata type 2.

Test Details

The DSP Gene Keratosis palmoplantaris striata type 2 NGS Genetic Test is a genetic test that utilizes NGS technology to analyze the DSP gene for mutations associated with Keratosis palmoplantaris striata type 2. This rare genetic disorder is characterized by thickening and scaling of the skin on the palms of the hands and soles of the feet.

NGS technology allows for the rapid and efficient sequencing of the entire coding region of the DSP gene, which encodes for the desmoplakin protein. Mutations in this gene can lead to the development of Keratosis palmoplantaris striata type 2.

The test involves obtaining a DNA sample, typically through a blood sample or a buccal swab. The DNA is then analyzed using NGS technology to identify any mutations or variations in the DSP gene.

The results of the test can help in confirming a diagnosis of Keratosis palmoplantaris striata type 2 and may also provide information about the specific mutation present in an individual. Genetic testing can be useful for individuals who have symptoms consistent with Keratosis palmoplantaris striata type 2, as well as for their family members who may be at risk of inheriting the condition.

It can help in providing a definitive diagnosis, guiding treatment decisions, and providing information about the risk of passing the condition on to future generations.

Test Components and Price

Components: DSP Gene Keratosis palmoplantaris striata type 2 Genetic Test

Price: 4400.0 AED

Sample Condition and Report Delivery

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Method and Test Type

Method: NGS Technology

Test Type: Osteology Dermatology Immunology Disorders

Doctor and Test Department

Doctor: Dermatologist

Test Department: Genetics

Pre Test Information

It is important to provide the clinical history of the patient who is going for the DSP Gene Keratosis palmoplantaris striata type 2 NGS Genetic DNA Test. A Genetic Counselling session may also be conducted to draw a pedigree chart of family members affected with the DSP Gene Keratosis palmoplantaris striata type 2 NGS Genetic DNA Test gene DSP.

Test Name DSP Gene Keratosis palmoplantaris striata type 2 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 DSP Gene Keratosis palmoplantaris striata type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DSP Gene Keratosis palmoplantaris striata type 2 NGS Genetic DNA Test gene DSP
Test Details

DSP Gene Keratosis palmoplantaris striata type 2 NGS Genetic Test is a genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the DSP gene for mutations associated with Keratosis palmoplantaris striata type 2. Keratosis palmoplantaris striata type 2 is a rare genetic disorder characterized by thickening and scaling of the skin on the palms of the hands and soles of the feet.

NGS technology allows for the rapid and efficient sequencing of the entire coding region of the DSP gene, which encodes for the desmoplakin protein. Mutations in this gene can lead to the development of Keratosis palmoplantaris striata type 2.

The test involves obtaining a DNA sample, typically through a blood sample or a buccal swab. The DNA is then analyzed using NGS technology to identify any mutations or variations in the DSP gene. The results of the test can help in confirming a diagnosis of Keratosis palmoplantaris striata type 2 and may also provide information about the specific mutation present in an individual.

Genetic testing can be useful for individuals who have symptoms consistent with Keratosis palmoplantaris striata type 2, as well as for their family members who may be at risk of inheriting the condition. It can help in providing a definitive diagnosis, guiding treatment decisions, and providing information about the risk of passing the condition on to future generations.