Hydranencephaly is a rare neurological condition characterized by the absence of cerebral hemispheres, which are replaced by sacs filled with cerebrospinal fluid. One specific form of this condition, known as Fowler type, has been linked to mutations in the FLVCR2 gene. DNA Labs UAE is at the forefront of diagnosing this genetic disorder through the FLVCR2 Gene Hydranencephaly Fowler Type Genetic Test. This comprehensive test is pivotal for families seeking answers about this rare condition, providing crucial information for managing and understanding the disease.
Symptoms of FLVCR2 Gene Hydranencephaly Fowler Type
Hydranencephaly Fowler type presents a range of symptoms that are critical for early diagnosis. These symptoms often manifest shortly after birth and may include:
- Microcephaly, where the head size is significantly smaller than that of other children of the same age and sex.
- Lack of growth or development of the cerebral cortex, leading to severe intellectual disability and developmental delays.
- Difficulty in feeding, including problems with swallowing or sucking.
- Respiratory issues, which can range from mild to severe.
- Involuntary muscle contractions, which can be sporadic or continuous.
- Seizures, which may vary in frequency and severity.
- A noticeable increase in the size of the skull due to the accumulation of cerebrospinal fluid.
It is imperative for parents and caregivers to be vigilant for these symptoms, as early detection can lead to better management of the condition.
FLVCR2 Gene Hydranencephaly Fowler Type Genetic Test
DNA Labs UAE offers a specialized genetic test designed to detect mutations in the FLVCR2 gene associated with hydranencephaly Fowler type. This test is a beacon of hope for many families, providing them with the answers they need to understand their child’s condition better. The process involves collecting a DNA sample through a simple and non-invasive method, ensuring a smooth and comfortable experience for all patients.
Understanding the Test Process
The genetic test for the FLVCR2 gene involves a series of steps to ensure accuracy and reliability. Initially, a detailed medical history of the patient and their family is taken to assess the risk and presence of genetic disorders. Following this, a DNA sample is collected, usually through a blood draw or a cheek swab. The sample is then analyzed in the laboratory, focusing on identifying mutations in the FLVCR2 gene that are indicative of hydranencephaly Fowler type. The results are thoroughly reviewed by genetic specialists, who provide a comprehensive report to the patient’s healthcare provider.
Cost of the Genetic Test
The cost of the FLVCR2 Gene Hydranencephaly Fowler Type Genetic Test at DNA Labs UAE is 4400 AED. This cost reflects the sophisticated technology and expertise required to conduct such a specialized test. While the price may seem significant, the value of the information it provides to affected families is immeasurable. It opens the door to tailored care plans and the possibility of connecting with support networks and resources specifically designed for families dealing with hydranencephaly Fowler type.
Conclusion
Hydranencephaly Fowler type is a challenging and complex condition, but with advances in genetic testing, families have a pathway to gaining crucial insights into their child’s health. The FLVCR2 Gene Hydranencephaly Fowler Type Genetic Test offered by DNA Labs UAE is a critical tool in this journey, providing not just answers but also hope. For more information on this test and to schedule an appointment, visit DNA Labs UAE.
