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Medical categories

Metabolic diseases (31 contents)

Amyloidosis [scrapie] (4 contents)

Hereditary or familial systemic scrofula, neuropathic form (1 content)

Hereditary or familial systemic scrofula, not specified (1 content)

Secondary organ amyloidoses (1 content)

Other amyloidoses (1 content)

Amyloidosis, not specified (3 contents)

Articles NEWS SPECIALIST ADVICE

Czech scientists have discovered a gene mutation that causes starchiasis

Researchers at Charles University in Prague have become the first in the world to find a mutation that may be responsible for AA amyloidosis (starchiasis).

Mysterious scrofula: what is it and how to treat it?

Starchiasis, or amyloidosis, is a disease whose main symptom is the accumulation of so-called amyloid in tissues and organs. Is the disease dangerous? What are the consequences of not treating...