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What is Benign Hereditary Chorea about?

Benign hereditary chorea (BHC) is a childhood-onset movement disorder caused by mutations in the NKX2.1 gene, characterized by non-progressive chorea and associated with brain-lung-thyroid syndrome. The review discusses clinical features, including atypical movement phenotypes, cognitive and psychiatric symptoms, and highlights the importance of genetic testing for better diagnosis and treatment strategies. It also examines the efficacy of available therapies and the expanding understanding of BHC as a deve

Author

huyenxiu2001

Language

EN