Herpes simplex keratitis (HSK) is a serious eye condition caused by the herpes simplex virus (HSV), particularly HSV-1. This viral infection affects the cornea, potentially…
Herpes simplex infection is a common viral condition caused by the herpes simplex virus (HSV). This virus exists in two primary forms: HSV-1, which is…
Herpes simplex hepatitis (HSH) is a rare yet severe viral infection caused by the herpes simplex virus (HSV). This condition predominantly affects immunocompromised individuals, pregnant…
Herpes Simplex Encephalitis (HSE) is a severe and potentially life-threatening condition caused by the herpes simplex virus (HSV), predominantly HSV-1. It is the most common…
Hereditary Factor XIII A subunit deficiency is a rare congenital bleeding disorder resulting from mutations in the F13A1 gene. This condition impairs the blood's ability…
Hereditary coproporphyria (HCP) is a rare genetic disorder characterized by a deficiency in the enzyme coproporphyrinogen oxidase (CPOX), which is crucial in the heme biosynthesis…
Hepatic coma, also known as stage 4 hepatic encephalopathy, is a severe and life-threatening condition resulting from liver failure. It occurs when toxins such as…
Heparin toxicity is a serious medical condition resulting from excessive administration of heparin, an anticoagulant commonly used to prevent blood clots. Understanding the causes, symptoms,…
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…