Short Description

NGS genetic DNA test detecets for variant and mutation detection in CERS3 gene for Ichthyosis, congenital, autosomal recessive, type 9

PreTest Information

Clinical History of Patient who is going for CERS3 Gene Ichthyosis, congenital, autosomal recessive, type 9 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CERS3 Gene Ichthyosis, congenital, autosomal recessive, type 9 NGS Genetic DNA Test gene CERS3

Detail Description

CERS3 Gene Ichthyosis

CERS3 Gene Ichthyosis is a rare genetic disorder that affects the skin. It is a type of congenital ichthyosis that is inherited in an autosomal recessive manner. This means that an individual must inherit two copies of the mutated gene, one from each parent, to develop the condition.

Symptoms

Individuals with CERS3 Gene Ichthyosis have dry, scaly, and thickened skin that may appear cracked or fissured. The skin may also be red, itchy, and irritated. In severe cases, the skin may become infected. The condition typically affects the entire body, including the face, scalp, and extremities.

Diagnosis

CERS3 Gene Ichthyosis can be diagnosed through genetic testing. A Next-Generation Sequencing (NGS) Genetic DNA Test can identify mutations in the CERS3 gene that cause the condition. This test is highly accurate and can provide a definitive diagnosis.

NGS Genetic DNA Test Cost

The cost of an NGS Genetic DNA Test for CERS3 Gene Ichthyosis in India is approximately INR 20,000. This test is available at DNA Labs India, a leading provider of genetic testing services in the country.

Contact DNA Labs India

If you or a loved one is experiencing symptoms of CERS3 Gene Ichthyosis, contact DNA Labs India for more information about genetic testing. Our team of experts can help you understand the condition, the testing process, and the available treatment options. We are committed to providing accurate and reliable genetic testing services to improve the health and well-being of our clients.

CERS3 (Ceramide Synthase 3) is a gene that encodes an enzyme involved in the synthesis of ceramides, which are lipid molecules essential for maintaining the skin's moisture and barrier function.

Mutations in the CERS3 gene can disrupt ceramide synthesis, leading to the development of Congenital Autosomal Recessive Ichthyosis Type 9.

NGS (Next-Generation Sequencing) genetic DNA tests can be used to analyze the DNA sequence of genes like CERS3 to identify any mutations or variants that may be associated with Congenital Autosomal Recessive Ichthyosis Type 9.

If you or someone you know is considering genetic testing for Congenital Autosomal Recessive Ichthyosis Type 9 related to the CERS3 gene, I recommend consulting with a dermatologist, a medical geneticist, or a genetic counselor. They can provide accurate and current information about the condition, the implications of genetic testing, and any available treatment or management options. Medical knowledge can evolve, so it's important to rely on expert guidance for the latest information.