罕見病多與變異或遺傳有關專家:早篩查早治療減重症 - 新城健康+ Web Interstitial Ad
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罕見病多與變異或遺傳有關專家:早篩查早治療減重症

近年不時聽到「罕見病」這個名字,其實目前全球已知的罕見病約有8,000多種,多數由基因變異或遺傳的基因缺陷導致。此症泛指患病率極低、患者人數極少的疾病。每年的4月15日是世界龐貝氏症日,而每年的4月則為法布瑞氏症關注月,今次帶大家認識這兩種罕見病的成因、病徵及治療方法,更有兩位相關病友分享生活點滴。

罕見病-龐貝氏症-法布瑞氏症

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