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Osteology Diseases
Symptoms and Testing information for ITGAM Gene Systemic Lupus Erythematosus Susceptibility to Genetic Test
Systemic Lupus Erythematosus (SLE) is a complex autoimmune disease characterized by the immune system attacking its own tissues, causing widespread inflammation and tissue damage in the affected organs. It can affect the joints, skin, brain, lungs, kidneys, and blood vessels, leading to a wide range of symptoms, some of which can be severe. Genetic factors […]
Symptoms and Testing information for FOXN1 Gene T-Cell Immunodeficiency Congenital Alopecia and Nail Dystrophy Genetic Test
— The FOXN1 gene plays a crucial role in the development and function of the immune system, particularly in the maturation of T-cells, which are essential for the body’s defense against infections and diseases. Mutations in the FOXN1 gene can lead to a rare but severe condition known as T-cell immunodeficiency, congenital alopecia, and nail […]
Symptoms and Testing information for GDF2 Gene Telangiectasia Hereditary Hemorrhagic Type 5 Genetic Test
Hereditary Hemorrhagic Telangiectasia (HHT) Type 5, associated with mutations in the GDF2 gene, is a genetic disorder that affects blood vessels. This condition leads to the development of abnormal blood vessels that can cause bleeding and other complications. Recognizing the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers […]
Symptoms and Testing information for ENG Gene Telangiectasia Hereditary Hemorrhagic of Rendu Osler and Weber Type 1 Genetic Test
Hereditary Hemorrhagic Telangiectasia (HHT), also known as Osler-Weber-Rendu Syndrome, is a genetic disorder that affects blood vessels and can cause bleeding in various parts of the body. It’s a condition characterized by the development of abnormal blood vessels that can lead to serious health issues. The ENG gene is one of the genes associated with […]
Symptoms and Testing information for ACVRL1 Gene Telangiectasia Hereditary Hemorrhagic Type 2 Genetic Test
Hereditary Hemorrhagic Telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is a genetic disorder that affects blood vessels and can lead to abnormal bleeding. The condition is characterized by the development of abnormal blood vessels such as arteriovenous malformations (AVMs) and telangiectasias. One of the genes associated with HHT is the ACVRL1 gene, which, when mutated, […]
Symptoms and Testing information for FLNA Gene Terminal Osseous Dysplasis Genetic Test
DNA Labs UAE is at the forefront of genetic testing and research, offering a comprehensive range of tests designed to detect various genetic conditions. Among these, the FLNA Gene Terminal Osseous Dysplasia Genetic Test is critical for diagnosing a rare but significant genetic disorder. This article delves into the symptoms of FLNA gene terminal osseous […]
