herpes simplex dendritic keratitis

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…
hereditary tyrosinemia type i

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

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 x deficiency disease

Hereditary Factor X Deficiency Disease

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…
her2 positive gastric adenocarcinoma

HER2-Positive Gastric Adenocarcinoma

HER2-positive gastric adenocarcinoma is a subtype of stomach cancer characterized by the overexpression of the HER2 (human epidermal growth factor receptor 2) protein. This aggressive…