PedAM
Pediatric Disease Annotations & Medicines
| Disease | n syndrome |
| Phenotype | C0155320|cortical blindness |
| Sentences | 3 |
| PubMedID- 22557993 | Clinical progression may disclose clues to underlying pathology: development of episodic memory impairment and involvement of other cognitive domains suggests ad; visual hallucinations, delusions, and parkinsonism may indicate dlb; asymmetric parkinsonism and ideomotor apraxia may suggest corticobasal degeneration, cbd; rapid progression of global disability, myoclonus, and cortical blindness with anton syndrome suggest prion disease (namely the heidenhain variant of creutzfeldt–jakob disease). |
| PubMedID- 24744933 | cortical blindness with anton syndrome (visual anosognosia) is characterized by denial of blindness by patient who is unable to see in the presence of intact anterior visual pathways. |
| PubMedID- 20299863 | Patient and methods: here we report a patient with complete permanent cortical blindness coupled with denial of the blindness (anton syndrome) as a result of bilateral occipital infarction. |
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