SCI Osteogenesis Imperfecta History Osteogenesis imperfecta (brittle bone disease) genetic dis allege characterized by increase fragility. Osteogenesis imperfecta is a heterogeneous group of inherited conditions arising from a smorgasbord of biochemical and morphological collagen defects. According to Tianmont the disease score been originated ternary yard years ago and can be traced bet on to the Egyptians done the centuries, we find a dislocated mummy of a chela of Ancient Egypt, a young Arab named Satib (Tainmont) the skeleton is compose dumb at the British museum. Nevertheless they discovered a Viking prince cognize as Boneless. Over the years serial of eponyms have been associated with The Osteogenesis imperfecta syndrome the terms OI Comgenita and OI Tarda (David Rowe, Jay Shapiro) where introduced by Losser in 1906 to indicated the age of rootage of fractures and to purpose the severity of the disease. The disease is as well as known as Vroliks syndrome beca use the prototypal type symptoms were recorded in 1842 by prof Willem Vrolik, professor of Anatomy, Pathological Anatomy and Zoology at the University of Amsterdam. Professor Vrolik depict in his Handbook of Pathological Anatomy (1842-1844), and a newborn sister with numerous fractures and hydrocephalus (1844-1849) (Baljet) .

According to Baljet Vrolik also mentioned that the infant lived three days and that both the parents were suffering from lues universalis at the time of birth (Baljet). In the more modern autobiography The origin Case of Osteogenesis imperfecta is credited to the french philosopher Ma lebranche in 1674 who inform a subject who ! appeared like a man mazed on a wheel (David Rowe, Jay Shapiro). The first detectable clinical translation of Osteogenesis imperfecta is presented in 1788 and found in the theses for the degree of medical specialty presented by Olof Jakob Ekman chief surgeon for the Swedish Royal martyrdom (David Rowe, Jay Shapiro). In 1979 David Sillence formulated the...If you want to get a in effect(p) essay, order it on our website:
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