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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Darier disease</span>&#8212;or&#44; more appropriately&#44; <span class="elsevierStyleItalic">Darier-White disease</span>&#8212;will perhaps be one of the few eponymous disease names that will survive in the dermatology of the future&#46; The eponym&#39;s survival will surely be assisted by the clear inappropriateness of the alternative names that have been proposed&#58; <span class="elsevierStyleItalic">keratosis follicularis</span> and&#44; more recently&#44; <span class="elsevierStyleItalic">dyskeratosis follicularis</span>&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">The last 2 decades have yielded key molecular and genetic knowledge&#46; The relationship between Darier disease and the <span class="elsevierStyleItalic">ATP2A2</span> gene and its chromosomal locus was clearly established&#44; and the aura of mystery surrounding this genodermatosis seemed to vanish&#46; But nothing could be further from reality&#58; the wealth of expression and the clinical and therapeutic unpredictability of Darier disease continue to fascinate us&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">The cases reported in this issue by Flores-Terry et al&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> provide a lovely example of the diversity of Darier disease&#46; They show that&#44; in parallel to&#8212;and even in spite of&#8212;advances in basic research&#44; clinical practice continues to attract and captivate us on a daily basis&#46; In fact&#44; suspicion of Darier disease based on those peculiar hemorrhagic blisters at acral sites is a good example of the old maxim&#44; &#8220;If you don&#8217;t think of it&#44; you won&#8217;t diagnose it&#44;&#8221; and it shows us the way to clinical excellence in dermatology&#46;</p></span>"
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