FIBROSIS RETROLENTAL PDF

bilateral retrolental fibrous masses which appeared during the first six retrolental fibroplasia are almost indistinguishable, since one . of the retina. As fibrosis. retrolental fibrosis, whereas he found 36 per cent in and, in , 45 per cent; this seems to be exceptional however. The affection as a rule manifests itself. Retinopathy of prematurity (ROP), also called retrolental fibroplasia (RLF) and Terry syndrome, is a disease of the eye affecting prematurely born babies.

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Retrolental fibroplasia | definition of retrolental fibroplasia by Medical dictionary

Before Terry’s time many sporadic cases of fibrosis behind the lens were reported. A great variety of descriptive terms were used, such as vascular cord in the vitreous, pseudoglioma, persistent hyaloid, atypical vitreous, persistent vitreous, fibrosis of the lens, microphthalmos, embryonic fibrous sheath of the lens and congenital retinal folds. There has been no increase in the sporadic forms of retrolental fibrosis.

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The past decade has shown a remarkable increase in what has been called “retrolental fibroplasia” in infants of premature birth. This increase is proportional to the degree of prematurity and the lowness of the birth weight, and it is selective in its geographic locality. The large group of infants and children fibrosiis this defect composes about. Privacy Policy Terms of Use.

Retinopathy of prematurity – Wikipedia

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