Short Description

NGS genetic DNA test detecets for variant and mutation detection in CCDC88C gene for Hydrocephalus, nonsyndromic, autosomal recessive type 1

PreTest Information

Clinical History of Patient who is going for CCDC88C Gene Hydrocephalus, nonsyndromic, autosomal recessive type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CCDC88C Gene Hydrocephalus, nonsyndromic, autosomal recessive type 1

Detail Description

Understanding CCDC88C Gene Hydrocephalus: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

Hydrocephalus is a medical condition characterized by the accumulation of excessive cerebrospinal fluid in the brain. This condition can lead to an increase in intracranial pressure, which can cause damage to the brain and impair its functions. Hydrocephalus can be caused by various factors, including genetic mutations.

One of the genetic mutations associated with hydrocephalus is the CCDC88C gene mutation. This mutation is classified as nonsyndromic, autosomal recessive type 1 hydrocephalus and is caused by a defect in the CCDC88C gene. The CCDC88C gene is responsible for producing a protein called GIV, which is involved in various cellular processes, including brain development.

Symptoms of CCDC88C Gene Hydrocephalus

The symptoms of CCDC88C gene hydrocephalus can vary depending on the severity of the condition. Some of the common symptoms include:

• Headache
• Nausea and vomiting
• Blurred vision
• Difficulty in walking or balancing
• Seizures
• Cognitive impairment

It is important to note that some of these symptoms can also be associated with other medical conditions. Therefore, it is important to consult a healthcare professional for an accurate diagnosis.

Diagnosis of CCDC88C Gene Hydrocephalus

The diagnosis of CCDC88C gene hydrocephalus typically involves a combination of physical examination, medical history review, and imaging tests. The imaging tests can include CT scan, MRI, or ultrasound. These tests can help identify the presence of excess cerebrospinal fluid and any abnormalities in the brain structure.

NGS Genetic DNA Test Cost for CCDC88C Gene Hydrocephalus

The Next-Generation Sequencing (NGS) Genetic DNA Test is a specialized genetic test that can help identify mutations in the CCDC88C gene associated with hydrocephalus. The cost of this test can vary depending on the testing facility and location.

At DNA Labs India, we offer NGS Genetic DNA Test for CCDC88C Gene Hydrocephalus at a cost of INR 20,000. This test is performed by our team of experienced geneticists using the latest technology and equipment to ensure accurate and reliable results.

Conclusion

CCDC88C gene hydrocephalus is a genetic condition that can cause the accumulation of excessive cerebrospinal fluid in the brain. This condition can lead to various symptoms, including headaches, seizures, and cognitive impairment. The diagnosis of this condition typically involves imaging tests, and the NGS Genetic DNA Test can help identify the specific genetic mutation associated with this condition.

If you suspect that you or a loved one may have CCDC88C gene hydrocephalus, it is important to consult a healthcare professional for an accurate diagnosis. At DNA Labs India, we offer specialized genetic testing services to help identify the underlying causes of various medical conditions, including hydrocephalus.