Abbreviation for pseudoxanthoma elasticum, a genetic disorder of elastic fiber degeneration with tiny areas of calcification in the skin, back of the eyes (retinae), and blood vessels. PXE is inherited from the parents, either as an autosomal recessive or as an autosomal dominant trait. PXE typically causes yellow-white small raised areas in the skin folds, often appearing in the second or third decades of life. These skin abnormalities frequently appear on the neck, armpits, and other areas that bend a great deal (referred to as flexure areas). The face is not affected by PXE. The doctor can often see abnormalities in the back of the eye (retinae) called angioid streaks, which are tiny breaks in the elastin-filled tissue there. These eye abnormalities can lead to blindness. Other areas that can be affected in PXE include the heart which can be affected by atherosclerosis and mitral valve prolapse. Small blood vessels are abnormally fragile in patients with PXE because the blood vessel walls contain elastin and are weakened. This can lead to abnormal bleeding in such areas as the bowel and, very rarely, the uterus. Impairment of circulation to the legs can lead to pains in the legs while walking (claudication).
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pseudoxanthoma elasticum

Medical dictionary. 2011.

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