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List of articles in "Disease" category - Page 391

Cholestasis

In medicine cholestasis is a condition where bile cannot flow from the liver to the duodenum. The two basic distinctions are an obstructive type of cholestasis where there is a […]


Trisomy 8

Trisomy 8 also known as Warkany syndrome 2 is a human chromosomal disorder caused by having three copies (trisomy) of chromosome 8. It can appear with or without mosaicism.


Birdshot chorioretinopathy

Birdshot chorioretinopathy is a rare form of bilateral posterior uveitis affecting the eye. It causes severe progressive inflammation of both the choroid and retina.Affected individuals are almost exclusively caucasian and […]


Lysinuric protein intolerance

Lysinuric protein intolerance (LPI) also called hyperdibasic aminoaciduria type 2cationic aminoaciduria or familial protein intolerance is an autosomal recessive metabolic disorder affecting amino acid transport. About 140 patients have been […]


Hypoaldosteronism

In medicine (endocrinology) hypoaldosteronism refers to decreased levels of the hormone aldosterone. The term isolated hypoaldosteronism is used to describe lowered aldosterone without corresponding changes in cortisol. (The two hormones […]


Bruit

Bruit (/ˈbruːt/) is the unusual sound that blood makes when it rushes past an obstruction (called turbulent flow) in an artery when the sound is auscultated with the bell portion […]


Pityriasis lichenoides chronica

Pityriasis lichenoides chronica (also known as Chronic guttate parapsoriasis Chronic pityriasis lichenoides Dermatitis psoriasiformis nodularis Parapsoriasis chronica and Parapsoriasis lichenoides chronica PLC) is an uncommon idiopathic acquired dermatosis characterized by […]


Boerhaave syndrome

Esophageal rupture (also known as Boerhaave’s syndrome) is rupture of the oesophageal wall. 56% of oesophageal perforations are iatrogenic usually due to medical instrumentation such as an endoscopy or paraoesophageal […]


Cowden syndrome

Cowden syndrome (also known as Cowden’s disease and Multiple hamartoma syndrome) is a rare autosomal dominant inherited disorder characterized by multiple tumor-like growths called hamartomas and an increased risk of […]


Basilar skull fracture

A basilar skull fracture (or basal skull fracture) is a fracture of the base of the skull typically involving the temporal bone occipital bone sphenoid bone and/or ethmoid bone.This type […]


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