Symptom onset of spinocerebellar ataxia type 10 in pregnancy and puerperium
Abstract Spinocerebellar ataxia type 10 is an autosomal dominant neurodegenerative disorder. It was initially described in Mexican families presenting with ataxia and epilepsy, with or without polyneuropathy, pyramidal signs and cognitive symptoms. The authors report three patients from the same fam...
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| Veröffentlicht in: | Journal of clinical neuroscience 2011-03, Vol.18 (3), p.437-438 |
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| container_title | Journal of clinical neuroscience |
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| creator | Teive, H.A.G Arruda, W.O Raskin, S Munhoz, R.P Zavala, J.A Werneck, L.C Ashizawa, T |
| description | Abstract Spinocerebellar ataxia type 10 is an autosomal dominant neurodegenerative disorder. It was initially described in Mexican families presenting with ataxia and epilepsy, with or without polyneuropathy, pyramidal signs and cognitive symptoms. The authors report three patients from the same family who were asymptomatic until gestation and puerperium, when they developed symptoms and signs suggestive of the syndrome. Genetic diagnosis was made in the three patients. The authors hypothesize that hormonal changes are likely to influence the manifestation of the condition. |
| doi_str_mv | 10.1016/j.jocn.2010.07.102 |
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It was initially described in Mexican families presenting with ataxia and epilepsy, with or without polyneuropathy, pyramidal signs and cognitive symptoms. The authors report three patients from the same family who were asymptomatic until gestation and puerperium, when they developed symptoms and signs suggestive of the syndrome. Genetic diagnosis was made in the three patients. The authors hypothesize that hormonal changes are likely to influence the manifestation of the condition.</description><identifier>ISSN: 0967-5868</identifier><identifier>EISSN: 1532-2653</identifier><identifier>DOI: 10.1016/j.jocn.2010.07.102</identifier><identifier>PMID: 21236683</identifier><language>eng</language><publisher>Scotland: Elsevier Ltd</publisher><subject>Adult ; Age of Onset ; Ataxin-10 ; Female ; Genetic Predisposition to Disease ; Humans ; Nerve Tissue Proteins - genetics ; Neurology ; Pedigree ; Postpartum Period ; Pregnancy ; Pregnancy Complications - diagnosis ; Pregnancy Complications - genetics ; Pregnancy Complications - physiopathology ; SCA10 ; Spinocerebellar ataxia type 10 ; Spinocerebellar Ataxias - diagnosis ; Spinocerebellar Ataxias - genetics ; Spinocerebellar Ataxias - physiopathology</subject><ispartof>Journal of clinical neuroscience, 2011-03, Vol.18 (3), p.437-438</ispartof><rights>Elsevier Ltd</rights><rights>2010 Elsevier Ltd</rights><rights>Copyright © 2010 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-eedae81ace384e351394981abdab8a5152f1f4d919e646a0f406318a40163c953</citedby><cites>FETCH-LOGICAL-c442t-eedae81ace384e351394981abdab8a5152f1f4d919e646a0f406318a40163c953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0967586810006016$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21236683$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Teive, H.A.G</creatorcontrib><creatorcontrib>Arruda, W.O</creatorcontrib><creatorcontrib>Raskin, S</creatorcontrib><creatorcontrib>Munhoz, R.P</creatorcontrib><creatorcontrib>Zavala, J.A</creatorcontrib><creatorcontrib>Werneck, L.C</creatorcontrib><creatorcontrib>Ashizawa, T</creatorcontrib><title>Symptom onset of spinocerebellar ataxia type 10 in pregnancy and puerperium</title><title>Journal of clinical neuroscience</title><addtitle>J Clin Neurosci</addtitle><description>Abstract Spinocerebellar ataxia type 10 is an autosomal dominant neurodegenerative disorder. It was initially described in Mexican families presenting with ataxia and epilepsy, with or without polyneuropathy, pyramidal signs and cognitive symptoms. The authors report three patients from the same family who were asymptomatic until gestation and puerperium, when they developed symptoms and signs suggestive of the syndrome. Genetic diagnosis was made in the three patients. The authors hypothesize that hormonal changes are likely to influence the manifestation of the condition.</description><subject>Adult</subject><subject>Age of Onset</subject><subject>Ataxin-10</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Neurology</subject><subject>Pedigree</subject><subject>Postpartum Period</subject><subject>Pregnancy</subject><subject>Pregnancy Complications - diagnosis</subject><subject>Pregnancy Complications - genetics</subject><subject>Pregnancy Complications - physiopathology</subject><subject>SCA10</subject><subject>Spinocerebellar ataxia type 10</subject><subject>Spinocerebellar Ataxias - diagnosis</subject><subject>Spinocerebellar Ataxias - genetics</subject><subject>Spinocerebellar Ataxias - physiopathology</subject><issn>0967-5868</issn><issn>1532-2653</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1r3DAYhEVpaTZJ_0APRbeevNH3yhAKJeSLBnpIchZa-XWRa0uuZJf630dm0xx6SE9Cw8wgPYPQR0q2lFB11m276MKWkSKQXdHYG7ShkrOKKcnfog2p1a6SWukjdJxzRwipBSfv0RGjjCul-QZ9u1-GcYoDjiHDhGOL8-hDdJBgD31vE7aT_eMtnpYRMCXYBzwm-BFscAu2ocHjDGmE5OfhFL1rbZ_hw_N5gh6vLh8ubqq779e3F1_vKicEmyqAxoKm1gHXArikvBZ1ue8bu9dWUsla2oqmpjUooSxpBVGcaivKn7mrJT9Bnw-9Y4q_ZsiTGXx262sDxDmbWooSkGr3X6cWBY5WlBYnOzhdijknaM2Y_GDTYigxK23TmZW2WWkbsisaK6FPz_XzfoDmJfIXbzGcHwxQcPz2kEx2HoKDxidwk2mif73_yz9x1_vgne1_wgK5i3MKBbShJjNDzP269zo3LUurldYTRc2kqw</recordid><startdate>20110301</startdate><enddate>20110301</enddate><creator>Teive, H.A.G</creator><creator>Arruda, W.O</creator><creator>Raskin, S</creator><creator>Munhoz, R.P</creator><creator>Zavala, J.A</creator><creator>Werneck, L.C</creator><creator>Ashizawa, T</creator><general>Elsevier Ltd</general><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>7TK</scope></search><sort><creationdate>20110301</creationdate><title>Symptom onset of spinocerebellar ataxia type 10 in pregnancy and puerperium</title><author>Teive, H.A.G ; Arruda, W.O ; Raskin, S ; Munhoz, R.P ; Zavala, J.A ; Werneck, L.C ; Ashizawa, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-eedae81ace384e351394981abdab8a5152f1f4d919e646a0f406318a40163c953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Age of Onset</topic><topic>Ataxin-10</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Humans</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Neurology</topic><topic>Pedigree</topic><topic>Postpartum Period</topic><topic>Pregnancy</topic><topic>Pregnancy Complications - diagnosis</topic><topic>Pregnancy Complications - genetics</topic><topic>Pregnancy Complications - physiopathology</topic><topic>SCA10</topic><topic>Spinocerebellar ataxia type 10</topic><topic>Spinocerebellar Ataxias - diagnosis</topic><topic>Spinocerebellar Ataxias - genetics</topic><topic>Spinocerebellar Ataxias - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Teive, H.A.G</creatorcontrib><creatorcontrib>Arruda, W.O</creatorcontrib><creatorcontrib>Raskin, S</creatorcontrib><creatorcontrib>Munhoz, R.P</creatorcontrib><creatorcontrib>Zavala, J.A</creatorcontrib><creatorcontrib>Werneck, L.C</creatorcontrib><creatorcontrib>Ashizawa, T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of clinical neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Teive, H.A.G</au><au>Arruda, W.O</au><au>Raskin, S</au><au>Munhoz, R.P</au><au>Zavala, J.A</au><au>Werneck, L.C</au><au>Ashizawa, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Symptom onset of spinocerebellar ataxia type 10 in pregnancy and puerperium</atitle><jtitle>Journal of clinical neuroscience</jtitle><addtitle>J Clin Neurosci</addtitle><date>2011-03-01</date><risdate>2011</risdate><volume>18</volume><issue>3</issue><spage>437</spage><epage>438</epage><pages>437-438</pages><issn>0967-5868</issn><eissn>1532-2653</eissn><abstract>Abstract Spinocerebellar ataxia type 10 is an autosomal dominant neurodegenerative disorder. It was initially described in Mexican families presenting with ataxia and epilepsy, with or without polyneuropathy, pyramidal signs and cognitive symptoms. The authors report three patients from the same family who were asymptomatic until gestation and puerperium, when they developed symptoms and signs suggestive of the syndrome. Genetic diagnosis was made in the three patients. The authors hypothesize that hormonal changes are likely to influence the manifestation of the condition.</abstract><cop>Scotland</cop><pub>Elsevier Ltd</pub><pmid>21236683</pmid><doi>10.1016/j.jocn.2010.07.102</doi><tpages>2</tpages></addata></record> |
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| subjects | Adult Age of Onset Ataxin-10 Female Genetic Predisposition to Disease Humans Nerve Tissue Proteins - genetics Neurology Pedigree Postpartum Period Pregnancy Pregnancy Complications - diagnosis Pregnancy Complications - genetics Pregnancy Complications - physiopathology SCA10 Spinocerebellar ataxia type 10 Spinocerebellar Ataxias - diagnosis Spinocerebellar Ataxias - genetics Spinocerebellar Ataxias - physiopathology |
| title | Symptom onset of spinocerebellar ataxia type 10 in pregnancy and puerperium |
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