Prognosis in CBS and CBD is shaped by specific motor and functional features, but many presumed indicators show inconsistent associations with survival, and future prospective studies are needed to improve prognostic accuracy and optimize care strategies, including timely palliative support.
While rehabilitation may offer functional benefits across atypical parkinsonian syndromes, high-quality evidence remains limited and the need for early, multidisciplinary, and disease-specific interventions to support mobility and safety is highlighted.
Hikaru Kamo, Satoru Amano, Isabelle K. Gerzenshtein et al.· Journal of Parkinson's Disea...· 0 citations
Moyamoya Angiopathy (MMA) is a rare, progressive, steno-occlusive cerebrovascular disorder. The disease can be idiopathic (Moyamoya Disease, MMD) or associated with heritable or acquired conditions (i.e., Moyamoya Syndrome, MMS). Among clinical symptoms of MMA, cognitive aspects are acknowledged but not well-characteri...
Serena Beretta, I. Scala, Isabella Canavero et al.· Neuropsychology Review· 0 citations
Individuals across the FTLD spectrum experience changes to communication that impact their social engagement and quality of life, and recommendations are provided based on the insights and group-level preferences reported here.
Gabriela F. Meade, B. Reinecker, Carrie F. Milliard et al.· American Journal of Speech-L...· 0 citations
Importance: Catatonia is a neuropsychiatric syndrome characterized by abnormalities in motor behavior, speech, volition, and affect. Although historically associated with schizophrenia, contemporary diagnostic frameworks recognize catatonia as a transdiagnostic condition occurring across psychiatric, medical, and neuro...
Namratha Mohan, A. Sarangi· The Primary Care Companion F...· 0 citations
PPP2R5D
-related neurodevelopmental disorder (Jordan syndrome) is a rare genetic condition characterized by developmental delay, intellectual disability, and macrocephaly. More recently, a small number of patients with
PPP2R5D
variants have been reported to develop dystonia-parkinsonism during adolescence or adult...
H. Kaushal, Akanksha Nagar, Balveen Singh et al.· Journal of Neurosciences in...· 0 citations
In this large clinical cohort, patients diagnosed with Korsakoff syndrome had a high burden of vascular comorbidities, frequent under-recognition of Wernicke encephalopathy, and substantial mortality, highlighting the need for earlier recognition and more standardized diagnostic evaluation of Korsakoff syndrome.
I. Coffi, Emmanuel Lecœur, K. Zarca et al.· JAMA Neurology· 1 citation
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