Skin and aortic samples from two patients who died by lethal perinatal Osteogenesis Imperfecta (O. I.) were studied by optical and electron microscopy and compared with similar samples from two normal human fetuses and one newborn child. No significant abnormalities were observed in the dermis of O. I. patients apart from small differences in the diameter of reticular collagen fibrils. On the contrary, in the aortas of both patients collagen fibrils were significantly smaller than in the controls; moreover, elastin lamellae were deeply altered and consisted of roundish aggregates of elastin, massively permeated by cytochemically recognizable glycosaminoglycans. As identical features were described in experimental lathyrism by using inhibitors of the enzyme lysyl oxidase (Pasquali Ronchetti et al., 1984), the conclusion is reached that in the two cases of lethal perinatal O. I. examined, a severe lysyl oxidase deficiency could account for the observed ultrastructural abnormalities of elastin and that, besides defects of collagen type I, additional alterations of cellular metabolism might be responsible for the clinical heterogeneity of the diesease. © 1986, Gustav Fischer Verlag · Stuttgart · New York. All rights reserved.

Aortic Elastin Abnormalities in Osteogenesis Imperfecta Type II / Ronchetti, Ip.; Quaglino, D.; Contri, Mb.; Tenconi, R.; Bressan, G. M.; Volpin, D.. - In: COLLAGEN AND RELATED RESEARCH. - ISSN 0174-173X. - 6:5(1986), pp. 409-421. [10.1016/S0174-173X(86)80017-6]

Aortic Elastin Abnormalities in Osteogenesis Imperfecta Type II

Quaglino D.;Contri MB.;
1986

Abstract

Skin and aortic samples from two patients who died by lethal perinatal Osteogenesis Imperfecta (O. I.) were studied by optical and electron microscopy and compared with similar samples from two normal human fetuses and one newborn child. No significant abnormalities were observed in the dermis of O. I. patients apart from small differences in the diameter of reticular collagen fibrils. On the contrary, in the aortas of both patients collagen fibrils were significantly smaller than in the controls; moreover, elastin lamellae were deeply altered and consisted of roundish aggregates of elastin, massively permeated by cytochemically recognizable glycosaminoglycans. As identical features were described in experimental lathyrism by using inhibitors of the enzyme lysyl oxidase (Pasquali Ronchetti et al., 1984), the conclusion is reached that in the two cases of lethal perinatal O. I. examined, a severe lysyl oxidase deficiency could account for the observed ultrastructural abnormalities of elastin and that, besides defects of collagen type I, additional alterations of cellular metabolism might be responsible for the clinical heterogeneity of the diesease. © 1986, Gustav Fischer Verlag · Stuttgart · New York. All rights reserved.
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5
409
421
Aortic Elastin Abnormalities in Osteogenesis Imperfecta Type II / Ronchetti, Ip.; Quaglino, D.; Contri, Mb.; Tenconi, R.; Bressan, G. M.; Volpin, D.. - In: COLLAGEN AND RELATED RESEARCH. - ISSN 0174-173X. - 6:5(1986), pp. 409-421. [10.1016/S0174-173X(86)80017-6]
Ronchetti, Ip.; Quaglino, D.; Contri, Mb.; Tenconi, R.; Bressan, G. M.; Volpin, D.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11380/1227185
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