Herpes Simplex Keratoconjunctivitis
Herpes simplex keratoconjunctivitis is an ocular condition caused by the herpes simplex virus (HSV), typically HSV-1. This viral infection primarily affects the cornea and conjunctiva,…
Herpes Simplex Keratitis: Causes, Symptoms, and Treatment
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: Causes, Symptoms
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: Causes, Symptoms
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
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…
Herpes Simplex Dendritic Keratitis
Herpes simplex dendritic keratitis is a common form of viral keratitis caused by the herpes simplex virus (HSV). This condition predominantly affects the cornea, leading…
Herniated Lumbar Disc: Causes, Symptoms
A herniated lumbar disc is a common spinal condition that occurs when the soft inner core of a spinal disc protrudes through its outer layer.…
Hereditary Tyrosinemia Type I
Hereditary Tyrosinemia Type I (HT1) is a rare genetic disorder caused by a deficiency in the enzyme fumarylacetoacetate hydrolase (FAH). This enzyme is essential in…
Hereditary Orotic Aciduria Type I
Hereditary orotic aciduria type I is a rare autosomal recessive metabolic disorder characterized by a deficiency in the enzyme uridine monophosphate synthase (UMPS). This condition…
Hereditary Factor XIII Deficiency Disease
Hereditary Factor XIII (FXIII) deficiency is a rare genetic bleeding disorder characterized by impaired blood clotting due to low levels or dysfunction of Factor XIII.…