Corino de AndradeBMJ 2005; 331 doi: https://doi.org/10.1136/bmj.331.7509.163 (Published 14 July 2005) Cite this as: BMJ 2005;331:163
Neurologist who discovered and gave his name to a hereditary form of amyloidosis
While working at the Santo António General Hospital in Porto (which had hired him as an unpaid neurologist to head the hospital's first department of neurology) Corino de Andrade noticed patients presenting with features that were characteristic of a peripheral neuropathy but did not fit any established clinical entity. During the next decade he came across dozens of similar cases and did extensive research on the epidemiology and pattern of transmission of this as yet unidentified disease.
In 1942 the autopsy of one of his patients revealed the presence of an amyloid substance in several body tissues. This led him to describe a new hereditary amyloid polyneuropathy—particularly prevalent not only in the fishing areas of northern Portugal, but also in coastal regions of other countries, including Japan and Sweden. This familial amyloid polyneuropathy type I (Portuguese) also became known as Corino de Andrade's disease.
Andrade's efforts were widely acknowledged by the international scientific community and attracted leading neurology gurus to Portugal. At a reception in Lisbon, …
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