Hemophilia is a rare genetic disorder in which blood does not clot properly due to insufficient clotting factors. Hemorrhaging in hemophilia can result in severe…
Hemorrhagic Disease of the Newborn (HDN), also known as Vitamin K Deficiency Bleeding (VKDB), is a potentially life-threatening condition that results from insufficient vitamin K…
Hemophilia B, also known as Christmas disease, is a rare inherited bleeding disorder caused by a deficiency of clotting factor IX. This condition leads to…
Hemophilia A is a genetic bleeding disorder caused by insufficient or defective clotting factor VIII. It is the most common type of hemophilia, affecting primarily…
Hemophagocytic lymphohistiocytosis (HLH) is a rare but potentially life-threatening immune disorder characterized by excessive immune activation. It leads to severe inflammation and multi-organ dysfunction. HLH…
Pyruvate kinase deficiency (PKD) is a rare genetic disorder that leads to chronic hemolytic anemia. This condition arises from a mutation in the PKLR gene,…
Hematopoietic Syndrome (HS) is a critical manifestation of Acute Radiation Syndrome (ARS) that primarily affects the bone marrow and blood-forming tissues. Exposure to high doses…
Hemangiomata of infancy are benign vascular tumors commonly seen in newborns and infants. These lesions are characterized by rapid growth during early months, followed by…
Helicobacter pylori gastritis is a common gastrointestinal condition caused by the infection of Helicobacter pylori bacteria in the stomach lining. This condition is a major…
Uterine leiomyoma, also known as fibroids, are non-cancerous tumors that develop in the uterus. These growths can vary in size, number, and location, significantly impacting…