Childhood-onset Huntignton ´s disease. A rare presentation

CONCLUSION: Childhood-onset HD differs from adult-form´s clinical manifestations. It should be considered in patients with progressive motor and cognitive impairment. Due to family inheritance, it is important to carefully examine family history and take it into account even without relatives affected, considering the anticipation phenomenon.PMID:38416505 | DOI:10.33588/rn.7805.2024039

Source: Revista de Neurologia - February 28, 2024 Category: Neurology Authors: A Gauto E Bellantonio P Pedernera-Bradichansky P Cafiero E Rodriguez P Massaro Source Type: research