Table 2.
Features of case-reports.
| Case-reports | Gender | Age of onset (years) | Origin/Type of visual deficit | Type of blindness | Psychotic features | Other remarks |
|---|---|---|---|---|---|---|
| Checkley and Slade, 1979 | F | 42 | Retinitis pigmentosa | LPB | Hallucinations | Partial hearing loss |
| Ogden, 1982 | M | >16 | Retinitis pigmentosa | LPB | Hallucinations, delusions | - |
| Grøndahl and Mjøen, 1986 | M | 62 | Retinitis pigmentosa | LPB | Yes | Psychosis is reported, but not schizophrenia Usher type I (deafblindness) |
| Engel et al., 1978 | F | 20 | Cortex | LCB | Catatonia | Partial complex status epilepticus3 |
| Sonavane et al., 2012 | F | 18 | Cortex | LCB | Yes | ECT-induced blindness |
| Sharfstein et al., 1999 | F | >60 | Cortex | LCB | Yes | Psychosis is reported, but not schizophrenia Severe dementia |
| Gobetz, 1967 | F | Birth | Optic atrophy | CPB | Hallucinations | - |
| Weiss et al., 1981 | F | ≃6 | Retinitis pigmentosa | EPB | Catatonia | Laurence-Moon-Bardet-Biedl syndrome |
| Catatonic schizophrenic-like psychosis | ||||||
| Kerschbaumer, 1943 | F4 | Birth | Eye under-development | CPB | No information | 3 cases are reported |
| Kay and Roth, 1961 | F | <82 | No information | late | Delusions | Partial hearing loss |
| Stewart and Sardo, 1965 | F | Birth | No information | Congenital | Catatonia | - |