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Late onset fulminant Wilson’s disease:A case report and review of the literature
Wilson’s disease(WD)is an autosomal recessive inherited disorder of hepatic copper metabolism.WD can be present in different clinical conditions,with the most common ones being liver disease and neuropsychiatric disturbances.Most cases present symptoms at<40years of age.However,few reports ex...
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Published in: | World journal of gastroenterology : WJG 2014-12, Vol.20 (46), p.17656-17660 |
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creator | Weitzman, Ella Pappo, Orit Weiss, Peretz Frydman, Moshe Haviv-Yadid, Yael Ben Ari, Ziv |
description | Wilson’s disease(WD)is an autosomal recessive inherited disorder of hepatic copper metabolism.WD can be present in different clinical conditions,with the most common ones being liver disease and neuropsychiatric disturbances.Most cases present symptoms at<40years of age.However,few reports exist in the literature on patients in whom the disease presented beyond this age.In this report,we present a case of late onset fulminant WD in a 58-year-old patient in whom the diagnosis was established clinically,by genetic analysis of the ATP7B gene disclosing rare mutations(G1099S and c.1707+3ins T)as well as by high hepatic copper content.We also reviewed the relevant literature.The diagnosis of WD with late onset presentation is easily overlooked.The diagnostic features and the geneticbackground in patients with late onset WD are not different from those in patients with early onset WD,except for the age.Effective treatments for this disorder that can be fatal are available and will prevent or reverse many manifestations if the disease is discovered early. |
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All rights reserved. 2014</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-4b581ec59646d3e7e71d1d4df78aba473093bde41ad7f8d7d14afa693fd97f2c3</citedby><cites>FETCH-LOGICAL-c443t-4b581ec59646d3e7e71d1d4df78aba473093bde41ad7f8d7d14afa693fd97f2c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265628/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265628/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25516681$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Weitzman, Ella</creatorcontrib><creatorcontrib>Pappo, Orit</creatorcontrib><creatorcontrib>Weiss, Peretz</creatorcontrib><creatorcontrib>Frydman, Moshe</creatorcontrib><creatorcontrib>Haviv-Yadid, Yael</creatorcontrib><creatorcontrib>Ben Ari, Ziv</creatorcontrib><title>Late onset fulminant Wilson’s disease:A case report and review of the literature</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>Wilson’s disease(WD)is an autosomal recessive inherited disorder of hepatic copper metabolism.WD can be present in different clinical conditions,with the most common ones being liver disease and neuropsychiatric disturbances.Most cases present symptoms at&lt;40years of age.However,few reports exist in the literature on patients in whom the disease presented beyond this age.In this report,we present a case of late onset fulminant WD in a 58-year-old patient in whom the diagnosis was established clinically,by genetic analysis of the ATP7B gene disclosing rare mutations(G1099S and c.1707+3ins T)as well as by high hepatic copper content.We also reviewed the relevant literature.The diagnosis of WD with late onset presentation is easily overlooked.The diagnostic features and the geneticbackground in patients with late onset WD are not different from those in patients with early onset WD,except for the age.Effective treatments for this disorder that can be fatal are available and will prevent or reverse many manifestations if the disease is discovered early.</description><subject>Adenosine Triphosphatases - genetics</subject><subject>Adenosine Triphosphatases - metabolism</subject><subject>Age of Onset</subject><subject>ATP7B</subject><subject>Biopsy</subject><subject>Case Report</subject><subject>Cation Transport Proteins - genetics</subject><subject>Cation Transport Proteins - metabolism</subject><subject>Copper-transporting ATPases</subject><subject>disease</subject><subject>DNA Mutational Analysis</subject><subject>Fatal Outcome</subject><subject>Female</subject><subject>Fulminant</subject><subject>gene</subject><subject>Genetic Predisposition to Disease</subject><subject>Hepatolenticular Degeneration - diagnosis</subject><subject>Hepatolenticular Degeneration - genetics</subject><subject>Hepatolenticular Degeneration - metabolism</subject><subject>Hepatolenticular Degeneration - therapy</subject><subject>Humans</subject><subject>Late</subject><subject>Liver - metabolism</subject><subject>Liver - pathology</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>onset</subject><subject>Phenotype</subject><subject>Predictive Value of Tests</subject><subject>Time Factors</subject><subject>Wilson’s</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNpVkcuKVDEQhoMoTjv6AG4kSzenze3k4kIYBm_QIIjiMqRP6nRnOJ30JDk9uPM1fD2fxLTTNppAqiB__VXUh9BzSpZcCf3q7mazPDCyDEIuqZK9fIAWjFHTMS3IQ7SghKjOcKYu0JNSbghhnPfsMbpgfU-l1HSBPq9cBZxigYrHedqF6GLF38JUUvz142fBPhRwBV5f4aEFnGGfcsUu-pYeAtzhNOK6BTyFCtnVOcNT9Gh0U4Fnp3iJvr57--X6Q7f69P7j9dWqG4TgtRPrXlMYeiOF9BwUKOqpF35U2q2dUJwYvvYgqPNq1F55KtzopOGjN2pkA79Eb-599_N6B36AWLOb7D6HncvfbXLB_v8Tw9Zu0sEK1lbFdDN4eTLI6XaGUu0ulAGmyUVIc7FUcmVMLwlpUnovHXIqJcN4bkOJPbKwjYVtLGxjYf-waDUv_p3vXPF3-U3AT6bbFDe3IW7OGkP08ZieCC1Mz9oVQh9f_huI4Ji7</recordid><startdate>20141214</startdate><enddate>20141214</enddate><creator>Weitzman, Ella</creator><creator>Pappo, Orit</creator><creator>Weiss, Peretz</creator><creator>Frydman, Moshe</creator><creator>Haviv-Yadid, Yael</creator><creator>Ben Ari, Ziv</creator><general>Baishideng Publishing Group Inc</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20141214</creationdate><title>Late onset fulminant Wilson’s disease:A case report and review of the literature</title><author>Weitzman, Ella ; Pappo, Orit ; Weiss, Peretz ; Frydman, Moshe ; Haviv-Yadid, Yael ; Ben Ari, Ziv</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-4b581ec59646d3e7e71d1d4df78aba473093bde41ad7f8d7d14afa693fd97f2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adenosine Triphosphatases - genetics</topic><topic>Adenosine Triphosphatases - metabolism</topic><topic>Age of Onset</topic><topic>ATP7B</topic><topic>Biopsy</topic><topic>Case Report</topic><topic>Cation Transport Proteins - genetics</topic><topic>Cation Transport Proteins - metabolism</topic><topic>Copper-transporting ATPases</topic><topic>disease</topic><topic>DNA Mutational Analysis</topic><topic>Fatal Outcome</topic><topic>Female</topic><topic>Fulminant</topic><topic>gene</topic><topic>Genetic Predisposition to Disease</topic><topic>Hepatolenticular Degeneration - diagnosis</topic><topic>Hepatolenticular Degeneration - genetics</topic><topic>Hepatolenticular Degeneration - metabolism</topic><topic>Hepatolenticular Degeneration - therapy</topic><topic>Humans</topic><topic>Late</topic><topic>Liver - metabolism</topic><topic>Liver - pathology</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>onset</topic><topic>Phenotype</topic><topic>Predictive Value of Tests</topic><topic>Time Factors</topic><topic>Wilson’s</topic><toplevel>online_resources</toplevel><creatorcontrib>Weitzman, Ella</creatorcontrib><creatorcontrib>Pappo, Orit</creatorcontrib><creatorcontrib>Weiss, Peretz</creatorcontrib><creatorcontrib>Frydman, Moshe</creatorcontrib><creatorcontrib>Haviv-Yadid, Yael</creatorcontrib><creatorcontrib>Ben Ari, Ziv</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>维普中文期刊数据库</collection><collection>维普中文医药期刊数据库</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - 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subjects | Adenosine Triphosphatases - genetics Adenosine Triphosphatases - metabolism Age of Onset ATP7B Biopsy Case Report Cation Transport Proteins - genetics Cation Transport Proteins - metabolism Copper-transporting ATPases disease DNA Mutational Analysis Fatal Outcome Female Fulminant gene Genetic Predisposition to Disease Hepatolenticular Degeneration - diagnosis Hepatolenticular Degeneration - genetics Hepatolenticular Degeneration - metabolism Hepatolenticular Degeneration - therapy Humans Late Liver - metabolism Liver - pathology Middle Aged Mutation onset Phenotype Predictive Value of Tests Time Factors Wilson’s |
title | Late onset fulminant Wilson’s disease:A case report and review of the literature |
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