Short Description

NGS genetic DNA test detecets for variant and mutation detection in RPL21 gene for Hypotrichosis type 12

PreTest Information

Clinical History of Patient who is going for RPL21 Gene Hypotrichosis type 12 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RPL21 Gene Hypotrichosis type 12 NGS Genetic DNA Test gene RPL21

Detail Description

RPL21 Gene Hypotrichosis Type 12 NGS Genetic DNA Test

Hypotrichosis type 12 is a rare genetic disorder that affects hair growth. It is caused by a mutation in the RPL21 gene, which plays a role in the production of proteins that are essential for hair growth. This disorder is inherited in an autosomal dominant manner, which means that a person only needs to inherit one copy of the mutated gene from either parent to develop the condition.

Symptoms of Hypotrichosis Type 12

The most common symptom of hypotrichosis type 12 is sparse hair growth, which begins in childhood or early adolescence. The hair is typically thin, brittle, and easily breakable. In addition to scalp hair, people with hypotrichosis type 12 may also have sparse or absent eyebrows, eyelashes, and body hair.

Diagnosis of Hypotrichosis Type 12

Diagnosis of hypotrichosis type 12 is typically based on clinical examination and genetic testing. A dermatologist or genetic counselor can perform a physical exam to evaluate the hair and scalp. Genetic testing can identify the specific mutation in the RPL21 gene that causes the disorder.

NGS Genetic DNA Test for Hypotrichosis Type 12

Next-generation sequencing (NGS) is a powerful tool for genetic testing that allows for the simultaneous analysis of multiple genes. NGS can be used to identify the specific mutation in the RPL21 gene that causes hypotrichosis type 12.

The cost of an NGS genetic DNA test for hypotrichosis type 12 in India is typically around INR 20,000. This cost may vary depending on the specific testing facility and any additional testing or counseling services that are included.

Conclusion

Hypotrichosis type 12 is a rare genetic disorder that affects hair growth. It is caused by a mutation in the RPL21 gene and is inherited in an autosomal dominant manner. Diagnosis of hypotrichosis type 12 is typically based on clinical examination and genetic testing. NGS genetic DNA testing can be used to identify the specific mutation in the RPL21 gene that causes the disorder. The cost of an NGS genetic DNA test for hypotrichosis type 12 in India is typically around INR 20,000.

It is important to seek medical advice if you or a family member are experiencing symptoms of hypotrichosis type 12. Genetic testing can help to confirm a diagnosis and provide information about the risk of passing the condition on to future generations.

At DNA Labs India, we offer a range of genetic testing services, including NGS genetic DNA testing for hypotrichosis type 12. Our team of experts can provide counseling and support throughout the testing process to ensure that you receive the most accurate and useful information possible.

Contact us today to learn more about our genetic testing services and how we can help you.