Neutropenia, a condition characterized by an abnormally low count of neutrophils, the most common type of white blood cells, is crucial in fighting off infections. Among its various types, Severe Congenital Neutropenia Type 6 (SCN6) stands out due to its genetic basis, specifically linked to mutations in the JAGN1 gene. This condition, inherited in an autosomal recessive manner, underscores the importance of genetic testing for early detection and management. DNA Labs UAE offers a comprehensive genetic test for this condition, aiming to provide crucial insights for affected families.
Symptoms of JAGN1 Gene Neutropenia Severe Congenital Type 6
The symptoms associated with JAGN1 Gene Neutropenia Severe Congenital Type 6 are diverse and significantly impact the quality of life of affected individuals. These symptoms include:
- Recurrent infections: Due to the reduced ability to fight off infections, individuals with this condition often experience frequent bacterial infections, which can be severe and difficult to treat.
- Oral ulcers and periodontal diseases: The low neutrophil count leads to an increased risk of oral health issues, including painful ulcers and gum diseases.
- Skin abscesses: The skin may also be a site for recurrent infections, resulting in abscesses that are challenging to heal.
- Otitis media: Middle ear infections are common, leading to discomfort and potential hearing loss if recurrent.
- Respiratory infections: The respiratory system can be severely affected, with individuals experiencing repeated episodes of pneumonia and bronchitis.
Early diagnosis and management of these symptoms are crucial to improving the quality of life for individuals with JAGN1 Gene Neutropenia Severe Congenital Type 6. This highlights the importance of genetic testing for at-risk families.
Genetic Test for JAGN1 Gene Neutropenia Severe Congenital Type 6
DNA Labs UAE offers a specialized genetic test to identify mutations in the JAGN1 gene, which is pivotal for families with a history of the condition or for those exhibiting symptoms. This test is not only a critical step in confirming the diagnosis but also aids in understanding the risk for potential siblings and future generations. The test involves a simple blood draw, and the sample is analyzed using advanced genetic sequencing technologies to identify mutations in the JAGN1 gene.
The cost of the JAGN1 Gene Neutropenia Severe Congenital Type 6 Autosomal Recessive Genetic Test at DNA Labs UAE is 4400 AED. While the cost may seem significant, the value it provides in terms of early diagnosis, potential treatment pathways, and family planning cannot be overstated.
For more information on the JAGN1 Gene Neutropenia Severe Congenital Type 6 Autosomal Recessive Genetic Test and to schedule a consultation, please visit https://dnalabsuae.com. Our team of experts is dedicated to providing comprehensive support and guidance throughout the testing process, ensuring that you and your family receive the care and information you need.
Understanding the genetic basis of conditions like JAGN1 Gene Neutropenia Severe Congenital Type 6 is a significant step forward in the realm of personalized medicine. With advancements in genetic testing, families affected by this condition have a powerful tool at their disposal for early detection, management, and planning for the future. DNA Labs UAE is committed to offering cutting-edge genetic testing services to help individuals and families navigate the complexities of genetic conditions with confidence and support.
