Short Description

NGS genetic DNA test detecets for variant and mutation detection in PCDH11X gene for Dyslexia

PreTest Information

Clinical History of Patient who is going for PCDH11X Gene Dyslexia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PCDH11X Gene Dyslexia

Detail Description

Understanding Dyslexia: PCDH11X Gene and NGS Genetic DNA Test

Dyslexia is a learning disorder that affects a person's ability to read, write, and spell. It is a common condition that affects up to 10% of the population worldwide. Dyslexia has been linked to various genes, including the PCDH11X gene. A genetic test that analyzes this gene can help diagnose dyslexia and provide insights into effective treatment.

What is the PCDH11X gene?

The PCDH11X gene is located on the X chromosome and plays a crucial role in brain development. This gene is responsible for producing a protein that helps neurons communicate with each other. Studies have shown that mutations or variations in the PCDH11X gene can affect how the brain processes language, leading to dyslexia.

How is dyslexia diagnosed?

Dyslexia is typically diagnosed through a series of tests that evaluate a person's reading and writing abilities. These tests may include:

• Phonological processing tests: These tests evaluate a person's ability to recognize and manipulate sounds in language.
• Reading fluency tests: These tests measure a person's reading speed and accuracy.
• Spelling tests: These tests evaluate a person's ability to spell words correctly.

In addition to these tests, a genetic test that analyzes the PCDH11X gene can provide valuable insights into the underlying cause of dyslexia.

NGS Genetic DNA Test for Dyslexia

Next-generation sequencing (NGS) genetic tests are a powerful tool for diagnosing dyslexia. These tests analyze a person's DNA to identify mutations or variations in the PCDH11X gene and other genes associated with dyslexia.

The NGS genetic DNA test for dyslexia involves taking a small sample of blood or saliva and analyzing it in a laboratory. The cost of this test in India is INR 20,000.

Symptoms of Dyslexia

The symptoms of dyslexia can vary from person to person and may include:

• Difficulty reading and writing
• Difficulty with phonological processing
• Difficulty with spelling
• Difficulty with comprehension
• Difficulty with organization and time management

If you or someone you know is experiencing these symptoms, it is important to seek a professional diagnosis and treatment.

Conclusion

Dyslexia is a common learning disorder that can have a significant impact on a person's life. The PCDH11X gene has been linked to dyslexia, and an NGS genetic DNA test can help diagnose this condition and provide valuable insights into effective treatment. DNA Labs India offers this test at a cost of INR 20,000. If you or someone you know is experiencing symptoms of dyslexia, it is important to seek a professional diagnosis and treatment.

For more information on NGS genetic DNA tests for dyslexia, contact DNA Labs India today.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for PCDH11X Gene Dyslexia NGS Genetic DNA Test