Membranous nephropathy with anti-tubular basement membrane antibody may be X-linked
The association of membranous nephropathy with Fanconi syndrome and anti-tubular basement antibodies appears to be a distinct subset of familial membranous nephropathy. We studied two Chinese families with four affected boys to evaluate the mode of inheritance of disease. HLA haplotype analysis of t...
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| Veröffentlicht in: | Pediatric nephrology (Berlin, West) West), 2000-08, Vol.14 (8-9), p.747-753 |
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| container_title | Pediatric nephrology (Berlin, West) |
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| creator | TAY, A. H. N REN, E.-C MURUGASU, B SIM, S.-K TAN, P.-H COHEN, A. H YAP, H.-K |
| description | The association of membranous nephropathy with Fanconi syndrome and anti-tubular basement antibodies appears to be a distinct subset of familial membranous nephropathy. We studied two Chinese families with four affected boys to evaluate the mode of inheritance of disease. HLA haplotype analysis of the family members in these two pedigrees did not reveal any significant linkages. However, microsatellite analysis of both pedigrees using markers on the X chromosome suggested linkage to the long arm of the X chromosome between the microsatellite markers DXS1001 and DXS1227. Identification and analysis of additional pedigrees may allow more precise mapping of the disease gene for anti-tubular basement membrane antibody-associated membranous nephropathy. |
| doi_str_mv | 10.1007/PL00013429 |
| format | Article |
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H. N ; REN, E.-C ; MURUGASU, B ; SIM, S.-K ; TAN, P.-H ; COHEN, A. H ; YAP, H.-K</creator><creatorcontrib>TAY, A. H. N ; REN, E.-C ; MURUGASU, B ; SIM, S.-K ; TAN, P.-H ; COHEN, A. H ; YAP, H.-K</creatorcontrib><description>The association of membranous nephropathy with Fanconi syndrome and anti-tubular basement antibodies appears to be a distinct subset of familial membranous nephropathy. We studied two Chinese families with four affected boys to evaluate the mode of inheritance of disease. HLA haplotype analysis of the family members in these two pedigrees did not reveal any significant linkages. However, microsatellite analysis of both pedigrees using markers on the X chromosome suggested linkage to the long arm of the X chromosome between the microsatellite markers DXS1001 and DXS1227. Identification and analysis of additional pedigrees may allow more precise mapping of the disease gene for anti-tubular basement membrane antibody-associated membranous nephropathy.</description><identifier>ISSN: 0931-041X</identifier><identifier>EISSN: 1432-198X</identifier><identifier>DOI: 10.1007/PL00013429</identifier><identifier>PMID: 10955919</identifier><identifier>CODEN: PENED3</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Autoantibodies - analysis ; Basement Membrane - immunology ; Basement Membrane - pathology ; Biological and medical sciences ; China ; Chromosome Mapping ; DNA Primers ; Female ; Genetic Markers ; Glomerulonephritis ; Glomerulonephritis, Membranous - genetics ; Glomerulonephritis, Membranous - immunology ; Glomerulonephritis, Membranous - pathology ; Haplotypes ; HLA Antigens - genetics ; Humans ; Infant ; Kidney Glomerulus - pathology ; Kidney Tubules - immunology ; Kidney Tubules - pathology ; Kidney Tubules, Proximal - physiopathology ; Male ; Medical sciences ; Microsatellite Repeats ; Nephrology. 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Renal failure ; Pedigree ; X Chromosome</subject><ispartof>Pediatric nephrology (Berlin, West), 2000-08, Vol.14 (8-9), p.747-753</ispartof><rights>2000 INIST-CNRS</rights><rights>IPNA - International Pediatric Nephrology Association New York, USA 2000</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c339t-501660f90e31cfb393f5f863407ffefcfdbb5960907a01ae0a4bd9b22e8f53f03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1445503$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10955919$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TAY, A. H. N</creatorcontrib><creatorcontrib>REN, E.-C</creatorcontrib><creatorcontrib>MURUGASU, B</creatorcontrib><creatorcontrib>SIM, S.-K</creatorcontrib><creatorcontrib>TAN, P.-H</creatorcontrib><creatorcontrib>COHEN, A. H</creatorcontrib><creatorcontrib>YAP, H.-K</creatorcontrib><title>Membranous nephropathy with anti-tubular basement membrane antibody may be X-linked</title><title>Pediatric nephrology (Berlin, West)</title><addtitle>Pediatr Nephrol</addtitle><description>The association of membranous nephropathy with Fanconi syndrome and anti-tubular basement antibodies appears to be a distinct subset of familial membranous nephropathy. We studied two Chinese families with four affected boys to evaluate the mode of inheritance of disease. HLA haplotype analysis of the family members in these two pedigrees did not reveal any significant linkages. However, microsatellite analysis of both pedigrees using markers on the X chromosome suggested linkage to the long arm of the X chromosome between the microsatellite markers DXS1001 and DXS1227. Identification and analysis of additional pedigrees may allow more precise mapping of the disease gene for anti-tubular basement membrane antibody-associated membranous nephropathy.</description><subject>Autoantibodies - analysis</subject><subject>Basement Membrane - immunology</subject><subject>Basement Membrane - pathology</subject><subject>Biological and medical sciences</subject><subject>China</subject><subject>Chromosome Mapping</subject><subject>DNA Primers</subject><subject>Female</subject><subject>Genetic Markers</subject><subject>Glomerulonephritis</subject><subject>Glomerulonephritis, Membranous - genetics</subject><subject>Glomerulonephritis, Membranous - immunology</subject><subject>Glomerulonephritis, Membranous - pathology</subject><subject>Haplotypes</subject><subject>HLA Antigens - genetics</subject><subject>Humans</subject><subject>Infant</subject><subject>Kidney Glomerulus - pathology</subject><subject>Kidney Tubules - immunology</subject><subject>Kidney Tubules - pathology</subject><subject>Kidney Tubules, Proximal - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microsatellite Repeats</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nephropathies. Renovascular diseases. Renal failure</subject><subject>Pedigree</subject><subject>X Chromosome</subject><issn>0931-041X</issn><issn>1432-198X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpd0E1LxDAQBuAgiruuXvwBUkQ8CNVJ0rTNURa_YEVBhb2VpJ2wXfuxJi3Sf2-0C4qnOeTJy8xLyDGFSwqQXD0vAIDyiMkdMqURZyGV6XKXTEFyGkJElxNy4Nzaq1Sk8T6ZUJBCSCqn5OURa21V0_YuaHCzsu1Gdash-Cy7VaCargy7XveVsoFWDmtsuqAef-DPs26LIajVEGgMlmFVNu9YHJI9oyqHR9s5I2-3N6_z-3DxdPcwv16EOeeyCwXQOAYjATnNjeaSG2HSmEeQGIMmN4XWQsYgIVFAFYKKdCE1Y5gawQ3wGTkfcze2_ejRdVlduhyryi_n78kSxgB8noen_-C67W3jd8sYYzz1jHl0MaLcts5ZNNnGlrWyQ0Yh--45--3Z45NtYq9rLP7QsVgPzrZAuVxVxheWl-7XRZEQwPkXvkKEYw</recordid><startdate>20000801</startdate><enddate>20000801</enddate><creator>TAY, A. H. 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Urinary tract diseases</topic><topic>Nephropathies. Renovascular diseases. Renal failure</topic><topic>Pedigree</topic><topic>X Chromosome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TAY, A. H. N</creatorcontrib><creatorcontrib>REN, E.-C</creatorcontrib><creatorcontrib>MURUGASU, B</creatorcontrib><creatorcontrib>SIM, S.-K</creatorcontrib><creatorcontrib>TAN, P.-H</creatorcontrib><creatorcontrib>COHEN, A. 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However, microsatellite analysis of both pedigrees using markers on the X chromosome suggested linkage to the long arm of the X chromosome between the microsatellite markers DXS1001 and DXS1227. Identification and analysis of additional pedigrees may allow more precise mapping of the disease gene for anti-tubular basement membrane antibody-associated membranous nephropathy.</abstract><cop>Heidelberg</cop><pub>Springer</pub><pmid>10955919</pmid><doi>10.1007/PL00013429</doi><tpages>7</tpages></addata></record> |
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| subjects | Autoantibodies - analysis Basement Membrane - immunology Basement Membrane - pathology Biological and medical sciences China Chromosome Mapping DNA Primers Female Genetic Markers Glomerulonephritis Glomerulonephritis, Membranous - genetics Glomerulonephritis, Membranous - immunology Glomerulonephritis, Membranous - pathology Haplotypes HLA Antigens - genetics Humans Infant Kidney Glomerulus - pathology Kidney Tubules - immunology Kidney Tubules - pathology Kidney Tubules, Proximal - physiopathology Male Medical sciences Microsatellite Repeats Nephrology. Urinary tract diseases Nephropathies. Renovascular diseases. Renal failure Pedigree X Chromosome |
| title | Membranous nephropathy with anti-tubular basement membrane antibody may be X-linked |
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