Symptoms and Testing information for ITGA2B Gene Thrombocytopenia Neonatal Alloimmune Genetic Test

Symptoms and Testing information for ITGA2B Gene Thrombocytopenia Neonatal Alloimmune Genetic Test

Symptoms of ITGA2B Gene Thrombocytopenia Neonatal Alloimmune Genetic Test Neonatal alloimmune thrombocytopenia (NAIT) is a significant blood disorder that affects newborns. It occurs when the mother’s immune system develops antibodies against fetal platelets, leading to their destruction. This condition is often associated with mutations in the ITGA2B gene, which plays a crucial role in platelet […]

Symptoms and Testing information for ITGB3 Gene Thrombocytopenia Neonatal Alloimmune Genetic Test

Symptoms and Testing information for ITGB3 Gene Thrombocytopenia Neonatal Alloimmune Genetic Test

Neonatal alloimmune thrombocytopenia (NAIT) is a critical condition that affects newborns, resulting from an incompatibility between the mother’s and the baby’s platelet antigens. This incompatibility leads to the mother’s immune system attacking the baby’s platelets, causing a significantly reduced platelet count in the newborn. One of the genetic markers associated with an increased risk of […]

Symptoms and Testing information for GATA1 Gene Thrombocytopenia X-Linked Genetic Test

Symptoms and Testing information for GATA1 Gene Thrombocytopenia X-Linked Genetic Test

Thrombocytopenia is a condition characterized by an abnormally low number of platelets in the blood, a crucial component for blood clotting and wound healing. Among the genetic forms of this condition, one notable type is linked to mutations in the GATA1 gene. This particular form of thrombocytopenia is inherited in an X-linked manner, primarily affecting […]

Symptoms and Testing information for WAS Gene Thrombocytopenia X-Linked Intermittent Genetic Test

Symptoms and Testing information for WAS Gene Thrombocytopenia X-Linked Intermittent Genetic Test

Symptoms of WAS Gene Thrombocytopenia X-Linked Intermittent Genetic Test Wiskott-Aldrich Syndrome (WAS) is a rare, genetic disorder that primarily affects males. It is characterized by thrombocytopenia (low platelet count), eczema, and an increased susceptibility to infections. The condition is caused by mutations in the WAS gene, which is located on the X chromosome, making it […]

Symptoms and Testing information for JAK2 Gene Thrombocytosis Familial JAK2 Related Genetic Test

Symptoms and Testing information for JAK2 Gene Thrombocytosis Familial JAK2 Related Genetic Test

Understanding the genetic underpinnings of various diseases has revolutionized the way we approach diagnosis and treatment. Among these, disorders associated with the JAK2 gene, particularly thrombocytosis, have garnered significant attention. Thrombocytosis, a condition characterized by an elevated platelet count, can be a precursor to more severe health issues, including blood clots, strokes, and heart attacks. […]

Symptoms and Testing information for F2 Gene Thrombophilia Due to Thrombin Defect Genetic Test

Symptoms and Testing information for F2 Gene Thrombophilia Due to Thrombin Defect Genetic Test

F2 gene thrombophilia, also known as Factor II gene mutation or prothrombin gene mutation, is a genetic condition that can significantly increase an individual’s risk of developing blood clots. This mutation affects the gene responsible for the production of prothrombin, a key protein in the blood clotting process. Individuals with this condition have a higher-than-normal […]

Symptoms and Testing information for HBD Gene Thalassemia Delta Genetic Test

Symptoms and Testing information for HBD Gene Thalassemia Delta Genetic Test

Thalassemia is a genetic blood disorder characterized by less oxygen-carrying hemoglobin and fewer red blood cells in the body than normal. Hemoglobin, the protein in red blood cells that carries oxygen, is made of two different parts: alpha globin and beta globin. The HBD gene is responsible for the production of delta globin, which is […]

Symptoms and Testing information for TBXAS1 Gene Thromboxane Synthase Deficiency Genetic Test

Symptoms and Testing information for TBXAS1 Gene Thromboxane Synthase Deficiency Genetic Test

At DNA Labs UAE, we understand the importance of accurate and timely genetic testing for the diagnosis and management of various genetic conditions. One such condition is Thromboxane Synthase Deficiency, caused by mutations in the TBXAS1 gene. This rare genetic disorder can have significant implications for affected individuals, and understanding its symptoms is crucial for […]

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