| Eponyms in category: Amyloid |
| 11
main and alternative
entries found.
|
|
| Andrade’s paramyeloidosis (Wohlwill-Andrade syndrome) |
| A hereditary form of amyloidosis characterized by predominantly neurological symptoms. |
| Andrade’s syndrome (Wohlwill-Andrade syndrome) |
| A hereditary form of amyloidosis characterized by predominantly neurological symptoms. |
| Andrade’s type of heritable polyneuropathy (Wohlwill-Andrade syndrome) |
| A hereditary form of amyloidosis characterized by predominantly neurological symptoms. |
| Corino de Andrade syndrome (Wohlwill-Andrade syndrome) |
| A hereditary form of amyloidosis characterized by predominantly neurological symptoms. |
| Königstein-Lubarsch syndrome (Lubarsch-Pick syndrome (Ludwig Pick)) |
| A rare syndrome characterized by the association of macroglossia with systematized amyloidosis of the skin and skeletal muscles. |
| Königstein-Lubarsch systematized, primitive amyloidosis (Lubarsch-Pick syndrome (Ludwig Pick)) |
| A rare syndrome characterized by the association of macroglossia with systematized amyloidosis of the skin and skeletal muscles. |
| Lubarsch-Königstein amyloidosis (Lubarsch-Pick syndrome (Ludwig Pick)) |
| A rare syndrome characterized by the association of macroglossia with systematized amyloidosis of the skin and skeletal muscles. |
| Lubarsch-Königstein disease (Lubarsch-Pick syndrome (Ludwig Pick)) |
| A rare syndrome characterized by the association of macroglossia with systematized amyloidosis of the skin and skeletal muscles. |
| Lubarsch-Pick syndrome (Ludwig Pick) |
| A rare syndrome characterized by the association of macroglossia with systematized amyloidosis of the skin and skeletal muscles. |
| Wohlwill-Andrade syndrome |
| A hereditary form of amyloidosis characterized by predominantly neurological symptoms. |
| Wohlwill-Corino Andrade syndrome (Wohlwill-Andrade syndrome) |
| A hereditary form of amyloidosis characterized by predominantly neurological symptoms. |
|
