Phenotype | Clinical features |
---|---|
Amnestic syndrome [13] | 1. Poor free recall 2. Decreased total recall (insufficient efficacy of cueing or impaired recognition) 3. Numerous intrusions |
lvPPA [15] | Both of the following core features must be present: 1. Impaired single-word retrieval in spontaneous speech and naming 2. Impaired repetition of sentences and phrases At least three of the following other features must be present: 1. Speech (phonologic) errors in spontaneous speech and naming 2. Spared single-word comprehension and object knowledge 3. Spared motor speech 4. Absence of frank agrammatism |
PCA [16] | At least three of the following must be present as early or presenting features ± evidence of their impact on activities of daily living: • Space perception deficit • Simultanagnosia • Object perception deficit • Constructional dyspraxia • Environmental agnosia • Oculomotor apraxia • Dressing apraxia • Optic ataxia • Alexia • Left/right disorientation • Acalculia • Limb apraxia (not limb-kinetic) • Apperceptive prosopagnosia • Agraphia • Homonymous visual field defect • Finger agnosia All of the following must be evident: • Relatively spared anterograde memory function • Relatively spared speech and nonvisual language functions • Relatively spared executive functions • Relatively spared behavior and personality |
CBS [17] | • Asymmetric dystonia • Focal or segmental myoclonus • Parkinsonian rigidity • Alien limb phenomena • Limb apraxia • Cortical sensory loss or dyscalculia • Frontal executive dysfunction • Visuospacial deficits |
Behavioral variant of frontal AD [18] | • Apathy • Disinhibition • Loss of empathy • Perseverative or compulsive behavior • Hyperorality • Dietary changes |
Dysexecutive variant of frontal AD [18] | • Decline in working memory • Decline in cognitive flexibility and inhibition • Absence of behavioral features of frontal AD |