{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T11:41:35Z","timestamp":1791286895513,"version":"4.1.0"},"reference-count":29,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2012,9,27]],"date-time":"2012-09-27T00:00:00Z","timestamp":1348704000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"crossref","award":["30370495"],"award-info":[{"award-number":["30370495"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"crossref"}]},{"name":"Programs Foundation of the Ministry of Education of China","award":["20090101110116"],"award-info":[{"award-number":["20090101110116"]}]},{"name":"Consortium for Clinical Investigation of Neurological Channelopathies of the National Institutes of Health","award":["U54-NS059065"],"award-info":[{"award-number":["U54-NS059065"]}]},{"name":"Consortium for Clinical Investigation of Neurological Channelopathies of the National Institutes of Health","award":["5-F05-NS065682"],"award-info":[{"award-number":["5-F05-NS065682"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Muscle and Nerve"],"published-print":{"date-parts":[[2013,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p><jats:italic>Introduction:<\/jats:italic> Hypokalemic periodic paralysis (HypoPP) is an autosomal dominant skeletal muscle ion channelopathy. Sex hormones are natural ion channel regulators. Different sex hormones have different effects on ion channels. A comparison of the penetrance and phenotype between males and females with HypoPP mutations should aid in proving that sex hormones play different roles in HypoPP and also provide the basis for the development of therapies against HypoPP. <jats:italic>Methods:<\/jats:italic> We identified all mutation carriers in 4 HypoPP families using PCR sequencing techniques. All patients underwent clinical investigation. <jats:italic>Results:<\/jats:italic> There were 8 men and 7 women mutation carriers in the 4 families. Male carriers had 100% penetrance, but female penetrance was only 28.57%. The highest attack frequency was 50\u2013150 times\/year for the men, whereas it was 30\u201350 times\/year for the women. The attacks disappeared during pregnancy. <jats:italic>Conclusions:<\/jats:italic> The penetrance and attack frequency were lower in women than in men with HypoPP mutations. 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