| 单词 |
familial amyloid polyneuropathy type i |
| 释义 |
familial amyloid polyneuropathy type I familial amyloid polyneuropathy type I An autosomal dominant form of hereditary amyloidosis that begins in early adulthood with rapidly progressive symmetrical sensorimotor polyneuropathy that quickly leads to incapacity. FAP I is now recognised as a permutation of transthyretin amyloidosis. |
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