PMC:6967083 / 1168-1632 JSONTXT

{"project":"AxD_symptoms","denotations":[{"id":"T4","span":{"begin":56,"end":70},"obj":"Phenotype"},{"id":"T5","span":{"begin":75,"end":88},"obj":"Phenotype"}],"attributes":[{"id":"A4","pred":"hp_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/HP_0002415"},{"id":"A5","pred":"hp_id","subj":"T5","obj":"http://purl.obolibrary.org/obo/HP_0002529"}],"text":"Alexander disease is a neurological disease that causes leukodystrophy and neuronal loss of brain, due to mutation of glial fibrillary acidic protein (GFAP) gene. When age of onset is high, bulbar symptoms and cerebellar dysfunctions develop gradually, requiring discrimination from adult-onset neurodegenerative disorders [1]. Herein, we report a unique case of genetically diagnosed Alexander disease comorbid, with clinically diagnosed Parkinson’s disease (PD)."}

{"project":"2_test","denotations":[{"id":"31952467-26023202-12806207","span":{"begin":324,"end":325},"obj":"26023202"}],"text":"Alexander disease is a neurological disease that causes leukodystrophy and neuronal loss of brain, due to mutation of glial fibrillary acidic protein (GFAP) gene. When age of onset is high, bulbar symptoms and cerebellar dysfunctions develop gradually, requiring discrimination from adult-onset neurodegenerative disorders [1]. Herein, we report a unique case of genetically diagnosed Alexander disease comorbid, with clinically diagnosed Parkinson’s disease (PD)."}