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List of articles in "Disease" category - Page 379

Bartonellosis

Bartonellosis is an infectious disease produced by bacteria of the genus Bartonella.Bartonella cause diseases such as Carrión´s disease trench fever cat-scratch disease bacillary angiomatosis peliosis hepatis chronic bacteremia endocarditis chronic […]


Glycogen storage disease type 0

Glycogen storage disease type 0 is a disease characterized by a deficiency in the glycogen synthase enzyme. Although glycogen synthase deficiency does not result in storage of extra glycogen in […]


Glycogen storage disease type III

Glycogen storage disease type III is an autosomal recessive metabolic disorder and inborn error of metabolism characterized by a deficiency in glycogen debranching enzymes.It is also known as Cori’s disease […]


Glycogen storage disease type IV

Glycogen storage disease type IV is a rare hereditary metabolic disorder.


Extravasation (intravenous)

Extravasation is the accidental administration of intravenously (IV) infused medications into the extravascular space/tissue around infusion sites either by leakage (e.g. because of brittle veins in very elderly patients) previous […]


Microscopic colitis

Microscopic colitis refers to two medical conditions which cause diarrhea: collagenous colitis and lymphocytic colitis. Both conditions are characterised by the following triad of clinicopathological features: Chronic watery diarrhoea; Normal […]


Ophthalmoparesis

Ophthalmoparesis or ophthalmoplegia refers to weakness (-paresis) or paralysis (-plegia) of one or more extraocular muscles which are responsible for eye movements. It is a physical finding in certain neurologic […]


Scleritis

Scleritis is a serious inflammatory disease that affects the white outer coating of the eye known as the sclera. The disease is often contracted through association with other diseases of […]


Neurofibroma

A neurofibroma is a benign nerve sheath tumor in the peripheral nervous system. Usually found in individuals with neurofibromatosis type I (NF1) an autosomal dominant genetically-inherited disease they can result […]


Hemoglobin C

Hemoglobin C (abbreviated as Hb C or HbC) is an abnormal hemoglobin in which substitution of a glutamic acid residue with a lysine residue at the 6th position of the […]


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