Hydrolethalus Syndrome is a rare genetic disorder that primarily affects the development of the fetus, leading to severe malformations and, in most cases, resulting in stillbirth or death shortly after birth. This condition is caused by mutations in the HYLS1 gene, which plays a crucial role in the early stages of embryonic development. Recognizing the symptoms associated with this genetic disorder is paramount for early diagnosis and understanding the potential risks for future pregnancies. At DNA Labs UAE, we offer a comprehensive HYLS1 Gene Hydrolethalus Syndrome Genetic Test to help families identify the mutation that leads to this condition.
Symptoms of Hydrolethalus Syndrome
Hydrolethalus Syndrome is characterized by a range of severe developmental abnormalities. The symptoms and physical manifestations can vary, but typically include the following:
- Malformations of the skull and brain, such as hydrocephalus (excess fluid in the brain), alobar holoprosencephaly (a condition where the brain fails to divide into lobes), and absence of the midline structures of the brain.
- Facial dysmorphisms, including a flat and elongated midface, cleft lip or palate, and a small jaw.
- Limb abnormalities, such as polydactyly (extra fingers or toes), syndactyly (fused fingers or toes), and clubfoot.
- Underdeveloped or absent nose.
- Respiratory issues due to underdeveloped lungs.
- Heart defects.
Due to the severity of these symptoms, most affected infants do not survive beyond the first few days or weeks of life. For families with a history of Hydrolethalus Syndrome, or those who have had a pregnancy affected by severe developmental issues, genetic testing can provide crucial information for future family planning.
HYLS1 Gene Hydrolethalus Syndrome Genetic Test at DNA Labs UAE
Understanding the genetic basis of Hydrolethalus Syndrome is essential for accurate diagnosis and counseling. The HYLS1 Gene Hydrolethalus Syndrome Genetic Test offered by DNA Labs UAE is designed to detect mutations in the HYLS1 gene that are responsible for this condition. Our state-of-the-art laboratory uses the latest genetic sequencing technologies to ensure accurate and reliable results.
The cost of the HYLS1 Gene Hydrolethalus Syndrome Genetic Test is 4400 AED. This comprehensive test is not only a critical tool for diagnosing affected individuals but also provides invaluable information for carriers and couples at risk of passing the condition to their offspring. Genetic counseling is recommended alongside testing to help families understand the results and discuss their reproductive options.
Why Choose DNA Labs UAE for Genetic Testing?
At DNA Labs UAE, we are committed to providing high-quality genetic testing services with accuracy, reliability, and confidentiality. Our team of experts is highly trained in the latest genetic testing methodologies and is dedicated to supporting families throughout the testing process. We understand the emotional and psychological impact of genetic disorders and strive to deliver compassionate care alongside our technical expertise.
Choosing DNA Labs UAE for your genetic testing needs ensures access to comprehensive testing services, expert interpretation of results, and support from a team that cares about your family’s health and well-being. Our HYLS1 Gene Hydrolethalus Syndrome Genetic Test is a vital resource for families seeking answers about this rare and challenging condition.
For more information about the HYLS1 Gene Hydrolethalus Syndrome Genetic Test or to schedule a consultation, please visit our website or contact us directly. Our team is here to provide the support and guidance you need to navigate the complexities of genetic testing and make informed decisions for your family’s future.
