IgA nephropathy historical perspective: Difference between revisions
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==Historical Perspective== | ==Historical Perspective== | ||
*[[IgA nephropathy]] was first described by Jean Berger, a pathologist, and Nicole Hinglais, an electron microscopist, in 1968 in France.<ref name="pmid4107073">{{cite journal| author=Berger J| title=IgA glomerular deposits in renal disease. | journal=Transplant Proc | year= 1969 | volume= 1 | issue= 4 | pages= 939-44 | pmid=4107073 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=4107073 }} </ref><ref name="pmid4180586">{{cite journal| author=Berger J, Hinglais N| title=[Intercapillary deposits of IgA-IgG]. | journal=J Urol Nephrol (Paris) | year= 1968 | volume= 74 | issue= 9 | pages= 694-5 | pmid=4180586 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=4180586 }} </ref><ref name="pmid21705126">{{cite journal| author=Feehally J, Cameron JS| title=IgA nephropathy: progress before and since Berger. | journal=Am J Kidney Dis | year= 2011 | volume= 58 | issue= 2 | pages= 310-9 | pmid=21705126 | doi=10.1053/j.ajkd.2011.03.024 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21705126 }} </ref>.). | *[[IgA nephropathy]] was first described by Jean Berger, a pathologist, and Nicole Hinglais, an electron microscopist, in 1968 in France.<ref name="pmid4107073">{{cite journal| author=Berger J| title=IgA glomerular deposits in renal disease. | journal=Transplant Proc | year= 1969 | volume= 1 | issue= 4 | pages= 939-44 | pmid=4107073 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=4107073 }} </ref><ref name="pmid4180586">{{cite journal| author=Berger J, Hinglais N| title=[Intercapillary deposits of IgA-IgG]. | journal=J Urol Nephrol (Paris) | year= 1968 | volume= 74 | issue= 9 | pages= 694-5 | pmid=4180586 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=4180586 }} </ref><ref name="pmid21705126">{{cite journal| author=Feehally J, Cameron JS| title=IgA nephropathy: progress before and since Berger. | journal=Am J Kidney Dis | year= 2011 | volume= 58 | issue= 2 | pages= 310-9 | pmid=21705126 | doi=10.1053/j.ajkd.2011.03.024 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21705126 }} </ref>.). | ||
*[[IgA nephropathy]] was originally described by Berger and Hinglais in 1968. In the original one-page article titled “Les depots intercapillaires d'IgA-IgG” in the “journal d’Urologie-Nephrologie”, the authors described the renal disease under light microscopy showing focal and segmental mesangial proliferation with expansion of the matrix. Under electron microscopy, they noted the predominance of [[IgA|IgA deposits]] in the renal mesangium that were associated with the presence of less significant presence of [[IgG]] and [[C3 (complement)|C3]]. | *[[IgA nephropathy]] was originally described by Berger and Hinglais in 1968. In the original one-page article titled “Les depots intercapillaires d'IgA-IgG” in the “journal d’Urologie-Nephrologie”, the authors described the renal disease under [[light microscopy]] showing focal and segmental [[Mesangium|mesangial]] proliferation with expansion of the matrix. Under [[electron microscopy]], they noted the predominance of [[IgA|IgA deposits]] in the [[Mesangium|renal mesangium]] that were associated with the presence of less significant presence of [[IgG]] and [[C3 (complement)|C3]]. | ||
*The association of [[IgA nephropathy]] with Henoch- | *The association of [[IgA nephropathy]] with [[Henoch-Schönlein purpura]] was made very shortly by Berger in 1969 following the first description of IgA nephropathy.<ref name="pmid4107073">{{cite journal| author=Berger J| title=IgA glomerular deposits in renal disease. | journal=Transplant Proc | year= 1969 | volume= 1 | issue= 4 | pages= 939-44 | pmid=4107073 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=4107073 }} </ref> | ||
==References== | ==References== |
Revision as of 15:26, 7 April 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Ali Poyan Mehr, M.D. [2] Associate Editor(s)-in-Chief: Olufunmilola Olubukola M.D.[3]
Overview
IgA nephropathy (Berger disease) was first described by Jean Berger, a pathologist, and Nicole Hinglais, an electron microscopist, in 1968 in France.
Historical Perspective
- IgA nephropathy was first described by Jean Berger, a pathologist, and Nicole Hinglais, an electron microscopist, in 1968 in France.[1][2][3].).
- IgA nephropathy was originally described by Berger and Hinglais in 1968. In the original one-page article titled “Les depots intercapillaires d'IgA-IgG” in the “journal d’Urologie-Nephrologie”, the authors described the renal disease under light microscopy showing focal and segmental mesangial proliferation with expansion of the matrix. Under electron microscopy, they noted the predominance of IgA deposits in the renal mesangium that were associated with the presence of less significant presence of IgG and C3.
- The association of IgA nephropathy with Henoch-Schönlein purpura was made very shortly by Berger in 1969 following the first description of IgA nephropathy.[1]
References
- ↑ 1.0 1.1 Berger J (1969). "IgA glomerular deposits in renal disease". Transplant Proc. 1 (4): 939–44. PMID 4107073.
- ↑ Berger J, Hinglais N (1968). "[Intercapillary deposits of IgA-IgG]". J Urol Nephrol (Paris). 74 (9): 694–5. PMID 4180586.
- ↑ Feehally J, Cameron JS (2011). "IgA nephropathy: progress before and since Berger". Am J Kidney Dis. 58 (2): 310–9. doi:10.1053/j.ajkd.2011.03.024. PMID 21705126.