Schizophrenia in a patient with cerebral autosomally dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL disease)

Nordic Journal of Psychiatry

Volumn 55, Issue 1, 2001, Pages 41-42

  Lagas, P A ^a   Juvonen, V ^a  

^a VAASA CENTRAL HOSPITAL   (Finland)

Author keywords

Cerebral autosomally dominant arteriopathy with subcortical infarcs and leucoencephalopathy; Chromosome 19; Notch3; Schizophrenia

Indexed keywords

NOTCH RECEPTOR;

ADULT; ARTERY DISEASE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN CORTEX; BRAIN INFARCTION; CASE REPORT; CHROMOSOME 19; COMORBIDITY; DEMENTIA; FEMALE; GENE MUTATION; HUMAN; LEUKOENCEPHALOPATHY; MEDICAL LITERATURE; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PSYCHOLOGIC TEST; SCHIZOPHRENIA;

ADULT; BRAIN; CHROMOSOME ABERRATIONS; DEMENTIA, MULTI-INFARCT; FEMALE; GENES, DOMINANT; HUMANS; MAGNETIC RESONANCE IMAGING; NEUROPSYCHOLOGICAL TESTS; POINT MUTATION; POLYMERASE CHAIN REACTION; PROTO-ONCOGENE PROTEINS; RECEPTORS, CELL SURFACE; RECEPTORS, NOTCH; SCHIZOPHRENIA;

EID: 0035081479     PISSN: 08039488     EISSN: None     Source Type: Journal    
DOI: 10.1080/080394801750093724     Document Type: Article

References (5)

1. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy: A positron emission tomography study in two affected family members
2. Analysis of Cadasil clinical natural history in a series of 136 patients belonging to 17 families linked to chromosome 19
3. No evidence for linkage between schizophrenia and eight microsatellite markers on chromosome 19
4. Genome scan of schizophrenia
5. Cerebral white matter disease in late-onset paranoid psychosis