In the realm of genetic testing, advancements have paved the way for early detection and management of various inherited disorders. One such condition that has garnered attention is Allan-Herndon-Dudley Syndrome (AHDS), a rare X-linked recessive disorder. AHDS is caused by mutations in the SLC16A2 gene, which plays a critical role in the development and function […]
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Symptoms and Testing information for GFAP Gene Alexander disease Genetic Test
Symptoms of GFAP Gene Alexander Disease Genetic Test Alexander disease is a rare and often fatal neurological disorder, which is one of a group of neurological conditions known as the leukodystrophies. These disorders affect the growth or maintenance of the myelin sheath, which is the fatty covering that insulates nerve fibers. Alexander disease is specifically […]
Symptoms and Testing information for DCPS Gene Al-Raqad syndrome Genetic Test
DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive suite of tests designed to identify a range of genetic conditions. Among these, the DCPS Gene Al-Raqad Syndrome Genetic Test is pivotal for diagnosing the rare and complex Al-Raqad syndrome. This article delves into the symptoms associated with Al-Raqad syndrome, the significance […]
Symptoms and Testing information for IFIH1 Gene Aicardi-Goutieres syndrome type 7 Genetic Test
Understanding the complexities of genetic disorders is crucial in the field of medical science, especially when it comes to rare conditions like Aicardi-Goutieres Syndrome (AGS). One of the genes associated with AGS is the IFIH1 gene, and mutations in this gene can lead to the development of Aicardi-Goutieres Syndrome Type 7. DNA Labs UAE offers […]
Symptoms and Testing information for ADAR Gene Aicardi-Goutieres syndrome type 6 Genetic Test
Aicardi-Goutieres Syndrome (AGS) is a rare genetic disorder that affects the brain, the immune system, and the skin. Type 6 of this syndrome, specifically, is caused by mutations in the ADAR gene. This condition is characterized by a variety of symptoms that can significantly impact the quality of life for those affected. Recognizing these symptoms […]
Symptoms and Testing information for SAMHD1 Gene Aicardi-Goutieres syndrome type 5 Genetic Test
Aicardi-Goutieres Syndrome (AGS) is a rare genetic disorder that affects the brain, immune system, and skin. Among the different types of AGS, Type 5 is particularly associated with mutations in the SAMHD1 gene. This condition is characterized by a range of symptoms that can significantly impact the quality of life of affected individuals and their […]
Symptoms and Testing information for RNASEH2A Gene Aicardi-Goutieres syndrome type 4 Genetic Test
In the intricate world of genetic disorders, Aicardi-Goutieres syndrome (AGS) stands out due to its complexity and the range of symptoms it presents. AGS is a rare, genetically inherited disease that mimics congenital viral infections without an actual infection, leading to significant neurological and immune system dysfunction. Among the genes associated with AGS, mutations in […]
Symptoms and Testing information for RNASEH2C Gene Aicardi-Goutieres syndrome type 3 Genetic Test
Aicardi-Goutieres Syndrome (AGS) is a rare genetic disorder that affects the brain, immune system, and skin. Among the different types of AGS, Type 3 is particularly associated with mutations in the RNASEH2C gene. This condition is known for its early onset, often presenting symptoms in infancy or early childhood, which can significantly impact the quality […]
Symptoms and Testing information for RNASEH2B Gene Aicardi-Goutieres syndrome type 2 Genetic Test
Aicardi-Goutieres Syndrome (AGS) is a rare genetic disorder that affects the brain, the immune system, and the skin. Among the various genes associated with this condition, mutations in the RNASEH2B gene lead to what is specifically known as AGS type 2. This particular type of AGS manifests through a range of symptoms that can significantly […]
Symptoms and Testing information for TREX1 Gene Aicardi-Goutieres syndrome type 1 Genetic Test
Aicardi-Goutieres Syndrome (AGS) is a rare genetic disorder that affects the brain, immune system, and skin. It is a condition that typically presents in infancy or early childhood and can result in a range of neurological and physical symptoms. One of the genes associated with this condition is the TREX1 gene, and mutations in this […]