Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-18T20:46:07.940Z Has data issue: false hasContentIssue false

Retinitis pigmentosa and schizophrenia

Published online by Cambridge University Press:  16 April 2020

C McDonald
Affiliation:
Institute of Psychiatry, Department of Psychological Medicine, de Crespigny Park, London SE5 8AF UK St John of God Hospital, Stillorgan, Co Dublin, Ireland
P Kenna
Affiliation:
Department of Genetics, Trinity College, Dublin 2
T Larkin
Affiliation:
St John of God Hospital, Stillorgan, Co Dublin, Ireland
Get access

Summary

There have been previous suggestions in the literature of a link between schizophrenia and retinitis pigmentosa (RP) or its associated syndromes. In this article, we describe two cases of schizophrenía and two cases of delusional disorder occurring in patients with RP. We explore possible reasons for an association between RP and schizophrenia including shared genetic predisposition, sensory deprivation, coarse brain disease and retinoid dysregulation. Awareness of an association may help to direct future research into the aetiology of these disorders, especially in the areas of neurochemistry and medical genetics.

Type
Case Report
Copyright
Copyright © Elsevier, Paris 1998

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Berson, ERosner, BSandberg, Met al.A randomised trial of vitamin A and vitamin E supplementation for retinitis pigmentosa Arch Ophthalmol 1993; 111: 761772CrossRefGoogle Scholar
Dryja, TPLi, TMolecular genetics of retinitis pigmentosa Hum Mot Genet 1995; 4: 17391743CrossRefGoogle ScholarPubMed
Eikmeier, GDieffenbach, RParanoide psychose bei angeborener Taubheit und Retinopathia pigmentosa (Usher-syndrom), Fallbericht Nervenarzt 1984; 55: 269270Google Scholar
Goodman, ABChromosomal locations and modes of action of genes of the retinoid (vitamin A) system support their involvement on the etiology of schizophrenia Am J Med Genet 1995; 60: 335348CrossRefGoogle ScholarPubMed
Gottesman, IIMoldin, SOSchizophrenia genetics at the millennium: cautious optimism Clin Genet 1997; 52: 404407CrossRefGoogle ScholarPubMed
Hallgren, BRetinitis pigmentosa combined with congenital deafness: with vestibulocerebellar ataxia and mental subnormality in a proportion of cases. A clinical and geneticostatistical study Acta Psychiatr Scand 34suppl 1381959 1101Google Scholar
Humphries, PFarrar, GJKenna, PMcWilliam, PRetinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease Clin Genet 1990; 38: 113CrossRefGoogle ScholarPubMed
Karjalainen, STerasvirta, MKarja, JKaariainen, HAn unusual otological manifestation of Usher's syndrome in four siblings Clin Genet 1983; 24: 273279CrossRefGoogle ScholarPubMed
Koizumi, JOfuku, KSakuma, KShiraishi, HIio, MNawano, SCNS changes in Usher's syndrome with mental disorder: CT, MRI and PET findings J Neurol Neurosurg Psychiatry 1988; 51: 987990CrossRefGoogle ScholarPubMed
Mangotich, MMisiaszek, JAtypical psychosis in Usher's syndrome Psychosomatics 1983; 24: 674675CrossRefGoogle ScholarPubMed
Murphy, KMOwen, MJSchizophrenia, CATCH 22 and FISH Br J Psychiatry 1996; 168: 397398CrossRefGoogle ScholarPubMed
Murphy, KMOwen, MJThe behavioural phenotype in velocardio-facial syndrome Am J Hum Genet 1997; 61: A5Google Scholar
Nuutila, ADystrophia retinae pigmentosa —dyacusis syndrome (DRD): a study of Usher or Hallgren syndrome J Genet Hum 1970; 18: 5788Google ScholarPubMed
Piazza, LFishman, GAKaplan, RDet al.Magnetic resonance imaging of central nervous system defects in Usher syndrome Retina 1987; 7: 241245CrossRefGoogle Scholar
Prager, SJeste, DVSensory impairment in late —life schizophrenia Schizophr Bull 1993; 19: 755772CrossRefGoogle ScholarPubMed
Schaefer, GBBodensteiner, JBThompson, JNet al.Volumetric neuroimaging of Usher syndrome: evidence of global involvement Am J Med Gen 1998; 79: 143.0.CO;2-T>CrossRefGoogle ScholarPubMed
Sharp, CWMuir, WJBlackwood, DHRWalker, MGosden, CSt Clair, DMSchizophrenia and mental retardation associated in a pedigree with retinitis pigmentosa and sensorineural deafness Am J Med Genet 1994; 54: 354360CrossRefGoogle Scholar
Small, JGDesmans, GMThe familial occurrence of retinitis pigmentosa, mental disorders and EEG abnormalities Am J Psychiatry 1966; 122: 12861289CrossRefGoogle ScholarPubMed
Stone, EMExpanding the repertoire of RP genes Nature Genetics 1998; 19: 311313CrossRefGoogle ScholarPubMed
Tamayo, MLBernal, JETamayo, GEet al.Usher syndrome: results of a screening programme in Colombia Clin Genet 1991; 40: 304311CrossRefGoogle Scholar
Tamayo, MLMaldonado, CPlaza, SLet al.Neuroradiology and clinical aspects of Usher syndrome Clin Genet 1996; 50: 126132CrossRefGoogle ScholarPubMed
Teunisse, RJCruysberg, JRMVerbeek, AZitman, FGThe Charles Bonnet syndrome: a large prospective study in the Netherlands Br J Psychiatry 1995; 166: 254257CrossRefGoogle ScholarPubMed
Todd, JA case of Laurence-Moon-Biedl syndrome with paranoid psychosis J Ment Defic 1955; 60: 331334Google ScholarPubMed
Tumer, THSchizophrenia and mental handicap: an historical review, with implications for further research Psychol Med 1989; 19: 301314Google Scholar
Vernon, MUsher's syndrome —deafness and progressive blindness. Clinical cases, prevention, theory and literature survey J Chron Dis 1969; 22: 133151CrossRefGoogle ScholarPubMed
Weiss, MMeshalum, BWijsenbeek, HThe possible relationship between Laurence-Moon-Biedl-Bardet syndrome and schizophrenic-like psychosis J Nerv Ment Dis 1981; 169: 259260CrossRefGoogle ScholarPubMed
Submit a response

Comments

No Comments have been published for this article.