Symptoms and Testing information for KRT16 Gene Palmoplantar Keratoderma Nonepidermolytic Focal Genetic Test

Symptoms and Testing information for KRT16 Gene Palmoplantar Keratoderma Nonepidermolytic Focal Genetic Test

Palmoplantar Keratoderma (PPK) represents a diverse group of disorders characterized by thickening of the skin on the palms of the hands and soles of the feet. Among the genetic forms of PPK, the nonepidermolytic focal type associated with mutations in the KRT16 gene is of significant interest due to its distinct clinical features and inheritance patterns. Understanding the symptoms of this condition is crucial for early diagnosis and management. Furthermore, genetic testing plays a pivotal role in confirming the diagnosis, guiding treatment options, and offering family counseling. DNA Labs UAE offers a comprehensive genetic test for this condition.

Symptoms of KRT16 Gene Palmoplantar Keratoderma Nonepidermolytic Focal

The symptoms of KRT16 gene Palmoplantar Keratoderma Nonepidermolytic Focal can vary among individuals but typically include the following:

  • Thickened Skin: The hallmark symptom of this condition is the thickening of the skin on the palms and soles, which can lead to discomfort and difficulty in hand and foot movements.
  • Cracks and Fissures: The affected areas may develop painful cracks and fissures that can bleed and lead to infections.
  • Redness and Inflammation: The skin on the palms and soles may appear red and inflamed, causing discomfort and itching.
  • Calluses and Corns: Due to the abnormal skin growth, individuals may also develop calluses and corns, which are areas of hardened skin that can be painful.
  • Reduced Sweating: The thickened skin can affect sweat gland function, leading to reduced sweating in the affected areas.

It’s important to note that symptoms can vary in severity and may evolve over time. Early diagnosis and management are crucial to alleviate symptoms and improve quality of life.

Genetic Testing for KRT16 Gene Mutation

Genetic testing for the KRT16 gene mutation is a definitive method for diagnosing Palmoplantar Keratoderma Nonepidermolytic Focal. DNA Labs UAE offers a specialized genetic test designed to identify mutations in the KRT16 gene. This test is crucial for confirming the diagnosis, especially in cases where clinical symptoms are ambiguous. Furthermore, it can provide valuable information for family planning and genetic counseling, as this condition is inherited in an autosomal dominant manner.

The cost of the genetic test at DNA Labs UAE is 4400 AED. The test involves a simple and non-invasive sample collection process, and results are provided in a comprehensive report that includes detailed findings and recommendations for management and follow-up.

For more information about the KRT16 gene Palmoplantar Keratoderma Nonepidermolytic Focal genetic test and to schedule your test, please visit DNA Labs UAE.

Early diagnosis and genetic testing are essential steps in managing Palmoplantar Keratoderma Nonepidermolytic Focal. By understanding the symptoms and utilizing available genetic testing resources, individuals and families affected by this condition can take proactive steps towards improved health and well-being.

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