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Friday, June 27, 2008
Beech Syndrome � Hereditary Disease With Autosomno-prepotent Type
Beech syndrome — hereditary disease With autosomno-prepotent type of inheritance. It is characterised by the congenital Changes character: early , , , with the small Molars. Expressed a nose and the next areas Persons about reddening of a skin and presence small pinkish it is marked At chronic , received the name red ё a nose. palms and stop often meets at , as one of displays a crisis. (illness of Vejr-Mitchella) — with expansion , shown Occurrence of burning pains, and a hypostasis in departments Finitenesses (more often bottom). a syndrome (synonyms: Chronic , a syndrome of the chronic hypertrophic ) — not clear aetiology, shown Symmetric puffiness and cyanosis of a skin of finitenesses and Fingers in a cold season; mainly young women are ill. At a phenomenon of Kassirera can be display of attacks or spontaneously to arise in the period. Local and night pains also are characteristic for dark blue spongy . Dark blue spongy — a version with primary localisation on a trunk and the top finitenesses.
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