{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,2]],"date-time":"2026-01-02T07:39:38Z","timestamp":1767339578865,"version":"build-2065373602"},"reference-count":13,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2013,10,30]],"date-time":"2013-10-30T00:00:00Z","timestamp":1383091200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Headache"],"published-print":{"date-parts":[[2014,5]]},"abstract":"<jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>CACNA1A<\/jats:italic>\n                      <\/jats:styled-content>\n                      gene disorders present a variable familial phenotype of ataxia, migraine with aura, and\/or hemiplegic migraine. Prevalence data for these conditions are scarce.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>\n                      The aim of this study is to report a minimal prevalence estimate for familial hemiplegic migraine with cerebellar ataxia and spinocerebellar ataxia type 6 in\n                      <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                      ortugal.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      This is a multisource population\u2010based prevalence study. Patients and families with spinocerebellar ataxia type 6 and familial hemiplegic migraine and cerebellar ataxia identified through the\n                      <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                      ortuguese survey of hereditary ataxias and spastic paraplegias were re\u2010evaluated. Prevalent patients were confirmed to be alive and affected at the 1st of\n                      <jats:styled-content style=\"fixed-case\">J<\/jats:styled-content>\n                      anuary 2013.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      One family with spinocerebellar ataxia type 6 and 2 families with other\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>CACNA1A<\/jats:italic>\n                      <\/jats:styled-content>\n                      gene mutations were identified. From these families, 23 patients were alive and living in\n                      <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                      ortugal in the prevalence day, for an estimated national prevalence per 100,000 inhabitants of 0.21 for familial hemiplegic migraine with cerebellar ataxia and of 0.01 for spinocerebellar ataxia type 6.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      The prevalence of familial hemiplegic migraine with cerebellar ataxia and spinocerebellar ataxia type 6 are both probably low in\n                      <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                      ortugal.\n                    <\/jats:p>\n                  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