Short Description

NGS genetic DNA test detecets for variant and mutation detection in FGFR1 gene for Kallmann syndrome type 2

PreTest Information

Clinical History of Patient who is going for FGFR1 Gene Kallmann syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR1 Gene Kallmann syndrome type 2 NGS Genetic DNA Test gene FGFR1

Detail Description

FGFR1 Gene Kallmann Syndrome Type 2 NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis

Kallmann Syndrome is a rare genetic disorder that affects the development of the hypothalamus and olfactory system. This disorder is caused by mutations in the FGFR1 gene. Kallmann Syndrome type 2 is caused by a mutation in the FGFR1 gene and is inherited in an autosomal dominant manner. This means that only one copy of the mutated gene is needed to develop the disorder.

What are the symptoms of Kallmann Syndrome Type 2?

The symptoms of Kallmann Syndrome Type 2 include:

• Delayed puberty
• Low levels of sex hormones
• Infertility
• Loss of sense of smell
• Abnormalities in the development of the face and teeth
• Abnormalities in the development of the reproductive system

How is Kallmann Syndrome Type 2 diagnosed?

Kallmann Syndrome Type 2 is diagnosed through genetic testing. NGS (Next Generation Sequencing) Genetic DNA Test is used to detect mutations in the FGFR1 gene. This test is highly accurate and can detect mutations in the gene with a high degree of sensitivity.

What is NGS Genetic DNA Test?

NGS Genetic DNA Test is a highly advanced genetic testing technique that uses next-generation sequencing technology to identify genetic mutations. This test is highly accurate and can detect mutations in the gene with a high degree of sensitivity. This test is used to diagnose a wide range of genetic disorders, including Kallmann Syndrome Type 2.

What is the cost of NGS Genetic DNA Test for Kallmann Syndrome Type 2?

The cost of NGS Genetic DNA Test for Kallmann Syndrome Type 2 in India is INR:20000. This is a reasonable price for a highly accurate and sensitive genetic test. The test is performed by DNA Labs India, a leading provider of genetic testing services in India.

Conclusion

Kallmann Syndrome Type 2 is a rare genetic disorder that affects the development of the hypothalamus and olfactory system. This disorder is caused by mutations in the FGFR1 gene and is inherited in an autosomal dominant manner. The symptoms of Kallmann Syndrome Type 2 include delayed puberty, low levels of sex hormones, infertility, loss of sense of smell, abnormalities in the development of the face and teeth, and abnormalities in the development of the reproductive system. NGS Genetic DNA Test is a highly accurate and sensitive genetic test that is used to diagnose Kallmann Syndrome Type 2. The cost of NGS Genetic DNA Test for Kallmann Syndrome Type 2 in India is INR:20000. DNA Labs India is a leading provider of genetic testing services in India.

If you suspect that you or a loved one may have Kallmann Syndrome Type 2, it is important to seek medical advice and genetic testing as soon as possible. Early diagnosis and treatment can help to manage the symptoms of this disorder and improve quality of life.