Ceroid lipofuscinosis neuronal type 3, commonly known as CLN3 disease or Batten disease, is a rare, inherited, neurodegenerative disorder that primarily affects the nervous system. Early symptoms typically begin in childhood, and the condition progressively leads to a severe decline in motor functions, vision, and mental capabilities. Given the severe impact of CLN3 disease, early diagnosis through genetic testing is crucial for managing symptoms and improving the quality of life for affected individuals. DNA Labs UAE offers a comprehensive genetic test for the CLN3 gene, aimed at providing an accurate diagnosis for families concerned about this condition.
Symptoms of CLN3 Disease
The symptoms of CLN3 disease can vary widely among individuals but generally follow a progressive course. Recognizing these symptoms early is vital for timely intervention and care management.
- Vision Loss: One of the earliest signs of CLN3 disease is vision impairment, leading to blindness. This results from the degeneration of cells in the retina.
- Movement Disorders: Affected individuals may experience coordination problems, muscle spasms, and involuntary movements, which worsen over time.
- Cognitive Decline: Progressive loss of intellectual functions, memory, and problem-solving abilities are common as the disease advances.
- Behavioral Changes: Personality changes, mood swings, and episodes of aggression or irritability may occur.
- Seizures: Many individuals with CLN3 disease develop seizures, which can vary in frequency and severity.
- Loss of Motor Skills: As the disease progresses, there is a significant decline in motor skills, leading to difficulties in walking and performing daily activities.
Genetic Testing for CLN3 Disease at DNA Labs UAE
DNA Labs UAE offers a specialized genetic test for the CLN3 gene to help diagnose Ceroid lipofuscinosis neuronal type 3. This test is crucial for families with a history of the disease or for those who have noticed the early symptoms in their children. The test involves a simple blood sample from which DNA is extracted and analyzed for mutations in the CLN3 gene.
Test Cost and Process
The cost of the CLN3 gene ceroid lipofuscinosis neuronal type 3 genetic test at DNA Labs UAE is 4400 AED. The process is streamlined and designed to be as convenient as possible for the individuals and families involved. Upon receiving the sample, the laboratory uses advanced genetic sequencing technologies to identify any mutations in the CLN3 gene that are indicative of the disease. Results are typically available within a few weeks, and a comprehensive report is provided to the patient’s healthcare provider for further consultation and management.
Why Choose DNA Labs UAE?
DNA Labs UAE is committed to providing accurate, reliable, and confidential genetic testing services. With a team of experienced geneticists and state-of-the-art technology, DNA Labs UAE ensures the highest standards of diagnostic accuracy. Additionally, the laboratory offers support and guidance throughout the testing process, helping families understand the implications of the test results and the next steps in managing the condition.
For more information on the CLN3 gene ceroid lipofuscinosis neuronal type 3 genetic test and to schedule your appointment, visit https://dnalabsuae.com/tests/cln3-gene-ceroid-lipofuscinosis-neuronal-type-3-genetic-test/.
Early diagnosis through genetic testing is crucial in managing CLN3 disease effectively. DNA Labs UAE is dedicated to providing the support and advanced diagnostic solutions needed to navigate this challenging condition, offering hope and assistance to affected families.
