Anticorpos e Huntington: Diagnóstico & tratamento

A doença de Huntington é uma desordem neurodegenerative genetically herdada causada por uma mutação dominante autosomal no gene do huntingtin tendo por resultado uma expansão da repetição do trinucleotide (CAG) com sobre 40 repetições.  

Cérebro normal e cérebro com doença de Huntington, mostrando ventrículos ampliados e atrofia do tecido de nervo e dos gânglio básicos. Crédito de imagem: Blamb/Shutterstock

Last Updated: Jan 23, 2019

Osman Shabir

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Osman Shabir

Osman is a Neuroscience PhD Research Student at the University of Sheffield studying the impact of cardiovascular disease and Alzheimer's disease on neurovascular coupling using pre-clinical models and neuroimaging techniques.

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