Short Description

NGS genetic DNA test detecets for variant and mutation detection in GDF3 gene for Klippel-Feil syndrome type 3, autosomal dominant

PreTest Information

Clinical History of Patient who is going for GDF3 Gene Klippel-Feil syndrome type 3, autosomal dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GDF3 Gene Klippel-Feil syndrome type 3, autosomal dominant NGS Genetic DNA Test gene GDF3

Detail Description

GDF3 Gene Klippel-Feil Syndrome Type 3: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

Klippel-Feil Syndrome (KFS) is a rare genetic disorder that affects the development of the spine. It is characterized by the fusion of two or more cervical vertebrae, which can lead to a variety of symptoms, including neck pain, stiffness, and limited range of motion. KFS can be caused by mutations in several different genes, including the GDF3 gene. In this article, we will focus on GDF3 Gene Klippel-Feil Syndrome Type 3, which is an autosomal dominant form of KFS.

Symptoms of GDF3 Gene Klippel-Feil Syndrome Type 3

The symptoms of GDF3 Gene Klippel-Feil Syndrome Type 3 can vary widely from person to person, even within families. Some of the most common symptoms include:

• Neck pain and stiffness
• Restricted range of motion in the neck
• Abnormal curvature of the spine
• Short neck
• Cleft palate
• Abnormalities of the ribs and/or vertebrae

Some people with GDF3 Gene Klippel-Feil Syndrome Type 3 may also experience neurological symptoms, such as numbness or weakness in the arms or legs, or problems with bladder or bowel function.

Diagnosis of GDF3 Gene Klippel-Feil Syndrome Type 3

Diagnosing GDF3 Gene Klippel-Feil Syndrome Type 3 can be challenging, as the symptoms can vary widely and may not be present in all affected individuals. However, there are several tests that can be used to help diagnose the condition:

• X-rays of the spine and neck
• Magnetic resonance imaging (MRI) of the spine and neck
• Genetic testing to look for mutations in the GDF3 gene

If you or someone you know is experiencing symptoms of GDF3 Gene Klippel-Feil Syndrome Type 3, it is important to speak with a healthcare professional who can help make an accurate diagnosis.

NGS Genetic DNA Test Cost for GDF3 Gene Klippel-Feil Syndrome Type 3

NGS (next-generation sequencing) genetic DNA testing is a powerful tool for diagnosing genetic disorders like GDF3 Gene Klippel-Feil Syndrome Type 3. This type of testing can identify mutations in the GDF3 gene that may be responsible for the condition.

The cost of NGS genetic DNA testing for GDF3 Gene Klippel-Feil Syndrome Type 3 can vary depending on the provider and the specific test being used. In India, the cost of NGS genetic DNA testing for this condition is typically around INR 20,000.

Conclusion

GDF3 Gene Klippel-Feil Syndrome Type 3 is a rare genetic disorder that can cause a variety of symptoms, including neck pain, stiffness, and restricted range of motion. If you or someone you know is experiencing these symptoms, it is important to speak with a healthcare professional who can help make an accurate diagnosis. NGS genetic DNA testing can be a powerful tool for diagnosing this condition, and the cost of testing in India is typically around INR 20,000.

At DNA Labs India, we offer a wide range of genetic testing services, including NGS genetic DNA testing for GDF3 Gene Klippel-Feil Syndrome Type 3. Contact us today to learn more about our services and how we can help you.

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 GDF3 Gene Klippel-Feil syndrome type 3, autosomal dominant NGS Genetic DNA Test