In 1998, Fabry in Germany and Anderson in the United Kingdom described for the first time and separately 2 patients with diffuse body angiokeratomas (angiokeratoma corporis diffusum).1,2 The first author was able to follow the evolution of his patient for almost 30 years, whereas Anderson could only make 1 report on his patient. Different from Fabry, though, Anderson described some signs and symptoms not related to dermatology. In 1958, Ruiter reported that only men were hemizygously affected,3 but on that same year, Colley et al proved involvement in women too.
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机译：1998年，德国的Fabry和英国的Anderson首次分别描述了2例弥漫性身体角膜血管瘤（angiokeratoma corporis diffusum）患者。1,2第一位作者能够追踪他的患者发展了近30年。 ，而安德森只能为他的病人做1次报告。但是，与法布里不同，安德森描述了一些与皮肤病学无关的体征和症状。 1958年，鲁伊特（Ruiter）报告说，只有男性受到半合子感染[3]，但在同一年，科尔利（Colley）等人也证明也参与了女性活动。
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