Abstract
It has been well documented that the nephrotic syndrome occurring in the 1st year of life corresponds to varied renal diseases. Omniglomerular diffuse mesangial sclerosis is an entity which was initially described by R. Habib (1, 2). The first patients described were four boys and two girls.
This is a preview of subscription content, log in via an institution to check access.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Habib R, Bois E (1973) Hétérogénéité des syndromes néphrotiques à début précoce du nourrisson. Helv Paediatr Acta 28: 91
Royer P, Habib R, Mathieu H, Broyer M (1975) Néphrologie Pêdiatrique. Flammarion médecine Editions, Paris, pp 190, 222
Kaplan BS, Bureau MA, Drummond KN (1974) The nephrotic syndrome in the first year of life: is a pathologic classification possible? J Pediatr 85: 615
Hallman N, Norio R, Rapola J (1973) Congenital nephrotic syndrome. Nephron 11: 101
Bouton JM, Coulter JBS (1974) The nephrotic syndrome of infancy. Acta Paediatr Scand 63: 769
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1982 Springer-Verlag Berlin Heidelberg
About this paper
Cite this paper
Bensman, A., Courpotin, C., Levy, M., Morel-Maroger, L., Mougenot, B., Addoti, F. (1982). Ommiglomerular Diffuse Mesangial Sclerosis: A Report of Three New Cases. In: Bulla, M. (eds) Renal Insufficiency in Children. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-68144-8_24
Download citation
DOI: https://doi.org/10.1007/978-3-642-68144-8_24
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-68146-2
Online ISBN: 978-3-642-68144-8
eBook Packages: Springer Book Archive