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…
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…
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 is a rare autosomal recessive metabolic disorder characterized by a deficiency in the enzyme uridine monophosphate synthase (UMPS). This condition…
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.…
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 Factor X Deficiency Disease is a rare genetic disorder characterized by impaired blood clotting due to insufficient or malfunctioning Factor X protein. This condition…
Hereditary Factor VII (FVII) deficiency is a rare genetic disorder characterized by insufficient levels or dysfunction of coagulation factor VII, a crucial protein involved in…