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1.
Neurocase ; 26(4): 220-226, 2020 08.
Article in English | MEDLINE | ID: mdl-32672088

ABSTRACT

We report a patient with alexia with agraphia for kanji after hemorrhage in the left posterior middle temporal gyrus. The results of single-character kanji reading and two-character on- (Chinese-style pronunciation), kun- (native Japanese pronunciation), and Jukujikun (irregular kun-) reading word tests revealed that the patient could not read kanji characters with on-reading but read the characters with kun-reading. We consider that this on-reading alexia was caused by disconnection between the posterior inferior temporal cortex (orthographic lexicon) and the posterior superior temporal gyrus (phonological lexicon), and preserved kun- and Jukujikun-reading was realized by bypassing the orthography-to-phonology route by the semantic route.


Subject(s)
Agraphia , Cerebral Hemorrhage , Dyslexia, Acquired , Pattern Recognition, Visual , Temporal Lobe , Aged , Agraphia/diagnosis , Agraphia/etiology , Agraphia/pathology , Agraphia/physiopathology , Cerebral Hemorrhage/complications , Cerebral Hemorrhage/diagnosis , Cerebral Hemorrhage/pathology , Cerebral Hemorrhage/physiopathology , Dyslexia, Acquired/diagnosis , Dyslexia, Acquired/etiology , Dyslexia, Acquired/pathology , Dyslexia, Acquired/physiopathology , Female , Humans , Magnetic Resonance Imaging , Pattern Recognition, Visual/physiology , Temporal Lobe/diagnostic imaging , Temporal Lobe/pathology , Temporal Lobe/physiopathology
3.
Dement Geriatr Cogn Dis Extra ; 6(3): 580-588, 2016.
Article in English | MEDLINE | ID: mdl-28203247

ABSTRACT

AIMS: The association between serum uric acid (UA) levels and cognitive function is controversial since UA can be a risk factor for cerebral ischemia as well as acting as a neuroprotective antioxidant. METHODS: We conducted a cross-sectional analysis of 228 elderly participants and examined neuropsychological test results, clinical data as well as brain magnetic resonance imaging data. PATIENTS: Overall, 64 participants were diagnosed with cognitive deterioration. To control for the effect of sex differences, 2 independent sets of single-variable and multivariate logistic regression analyses were performed with quartiles divided into non-sex-specific and sex-specific cutoff values for UA. RESULTS: In non-sex-specific quartiles, the participants in the highest quartiles of UA levels were found to be at a significantly higher risk of cognitive deterioration than those in the lowest quartiles. In sex-specific quartiles, the highest quartile showed an increased risk of cognitive deterioration, and a greater than fourfold increase in the risk in the highest quartiles was confirmed using multivariate regression models. However, no significant association was observed between serum UA levels and the presence of white matter lesions. CONCLUSIONS: Elevated serum UA levels were independently associated with cognitive deterioration. UA might have unknown adverse effects on cognitive function, other than causing vascular pathology.

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