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In the highlands of Papua New Guinea in the 1950s and 60s it was noticed that people (mostly women) of the Fore tribe were dying of what was originally thought to be a genetic disorder since it happened among family members.
The disease stole away the affected person’s ability to talk, walk and eat and to eventually die a shivering death.
We now know that this was kuru –a transmissible spongiform encephalopathy (TSE) or prion disease, same as Creutzfeldt-Jakob disease, mad cow disease in cattle, scrapie in sheep and chronic wasting seen in elk.
Joining me today to talk about the fascinating story of kuru is Chandana Bala. Chandy is the President of Global Insight Advisory Network and writes on the intersection of healthcare and technology. She is also a frequent writer for Gideon Informatics.
Watch the interview:
Listen to the audio:
Related:
France: Temporary suspension of prion research after death of lab technician
Prion diseases: Possible effective treatment strategy in new research
‘Camel Prion Disease’ discovered in dromedaries in Algeria: Study
Creutzfeldt-Jakob Disease (CJD) and other prion diseases
Creutzfeldt-Jakob disease (CJD): Treatment shows ‘very encouraging’ early results
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