{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,18]],"date-time":"2026-01-18T23:40:17Z","timestamp":1768779617670,"version":"3.49.0"},"reference-count":30,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2011,11,3]],"date-time":"2011-11-03T00:00:00Z","timestamp":1320278400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Eur J Clin Investigation"],"published-print":{"date-parts":[[2012,4]]},"abstract":"<jats:sec><jats:label\/><jats:p>Eur J Clin Invest 2012; 42 (4): 455\u2013462<\/jats:p><\/jats:sec><jats:sec><jats:title>Abstract<\/jats:title><jats:p><jats:bold>Background\u2002<\/jats:bold> Fabry disease (FD) is a rare X\u2010linked lysosomal storage disorder leading to an accumulation of globotriaosylceramides in the lysosomes of various organs.<\/jats:p><jats:p><jats:bold>Design\u2002<\/jats:bold> Being X\u2010chromosomal\u2010linked, most studies in the past have focused on involvement in male patients. However, it has been elucidated recently that female patients can present typical organ involvement and thus need to be treated, respectively.<\/jats:p><jats:p><jats:bold>Conclusions\u2002<\/jats:bold> This review wants to give a systematical overview of the typical organ involvement in female patients with FD. 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