Researchers are looking for genes that might increase a person’s risk of developing PSP. Scientists are studying gene-environment interaction – in which environmental factors and genetics may contribute to disease susceptibility for many diseases in which there may be genetic influences that differ among families or even in a single family. Investigators are integrating research tools involved with human genetics and disease epidemiology to better understand the joint risk factors that may contribute to the cause of PSP.
Recent approaches to therapeutic development for PSP have focused primarily on the clearance of abnormally accumulated tau in the brain. One ongoing clinical trial will determine the safety and tolerability of a compound that prevents accumulation of tau in preclinical models. Other studies are exploring improved tau imaging agents that will be used to assess disease progression and improvement in response to treatment.
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.This was my journey off PSP with my Husband it may be able to help some of you are new to this to let you know what PSP is all about..... I was my husbands carer,he was diagnosed with PSP in 2009 after 2 years of trying to find out what was wrong wi...
my dad was sadly diagnosed with psp on Jan 31st 2014, he had been having symptoms for at least 5 years.
sadly my dad passed away on 16th October this year.
Unfortunately I am on here marking 2 diseases on the map one for my mother who suffers from Corticobasal Degeneration (CBD) and another for my 12 (almost 13) year old niece who has Cystic Fibrosis. My family have been through so much we lost dad las...
My mom was diagnosed with CBD (Corticobasal Degeneration) in the summer of 2009 although some symptoms started showing as early as 2007 and finally died in August 2013. I have created a blog in Greek about the disease to try to inform other Greeks ...