Human cytomegalovirus is a species of the Cytomegalovirus genus of viruses which in turn is a member of the viral family known as Herpesviridae or herpesviruses. It is typically abbreviated […]
List of articles in "Disease" category - Page 254
Polycystic liver disease
Polycystic liver disease (PLD) usually describes the presence of multiple cysts scattered throughout normal liver tissue in association with polycystic kidney disease.
Fibrocystic breast changes
Fibrocystic breast or fibrocystic breast disease is a condition of breast tissue affecting an estimated 30-60% of women and at least 50% of women of childbearing age. It is characterized […]
Acne medicamentosa
Acne medicamentosa (commonly referred to as drug-induced acne) is acne that is caused or aggravated by medication. Because acne is generally a disorder of the pilosebaceous units caused by hormones […]
Acne cosmetica
Acne cosmetica is a term referring to acne caused by or aggravated by cosmetics. The mechanism was presumably a chemically induced plugging of the pilosebaceous orifice.
Tinea nigra
Tinea nigra (also known as superficial phaeohyphomycosis and Tinea nigra palmaris et plantaris) is a superficial fungal infection that causes dark brown to black painless patches on the palms of […]
Rokitansky–Aschoff sinuses
Rokitansky–Aschoff sinuses also entrapped epithelial crypts are pseudodiverticula or pockets in the wall of the gallbladder. They may be microscopic or macroscopic.Histologically they are outpouchings of gallbladder mucosa into the […]
Neuropathy ataxia and retinitis pigmentosa
Neuropathy ataxia and retinitis pigmentosa (NARP) is a condition that causes a variety of signs and symptoms chiefly affecting the nervous system. Beginning in childhood or early adulthood most people […]
Ornithine translocase deficiency
Ornithine translocase deficiency also called Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome is a rare autosomal recessive urea cycle disorder affecting the enzyme ornithine translocase which causes ammonia to accumulate in the blood a […]
Glutathione synthetase deficiency
Glutathione synthetase deficiency is a rare autosomal recessive metabolic disorder that prevents the production of glutathione. Glutathione helps prevent damage to cells by neutralizing harmful molecules generated during energy production. […]