Number： 002

Publication date： 2018/12/15

Content description： FAP（Familial Amyloid Polyneuropathy，澱粉樣多發性神經病變）是一種罕見的家族染色體顯性遺傳疾病，因為某些蛋白的基因突變，導致其結構出現變化，使得這些原本為水溶性的蛋白形成澱粉纖維在細胞外沉積而致病。

本小冊子由FAP（家族性澱粉樣多發性神經病變）病人互助小組及香港罕見疾病聯盟製作。

Number： 001

Publication date： 2020/06/01

Content description： Established in December 2014, Rare Disease Hong Kong (RDHK), is a charitable institution recognized by the government (ref. no.: 91/16233). It is first patient group in Hong Kong comprising cross-rare-disease patients and their families with the support of experts and academics in the field. You can learn more about us and rare diseases from this leaflet.

This leaflet was published by Rare Disease Hong Kong.