Cargando…

Marfan syndrome and schizophrenia : a case report and literature review

INTRODUCTION: Marfan syndrome is an autosomal dominant systemic disorder with connective tissue defects in multiple organ systems. Cardinal manifestations of this syndrome involve the cardiovascular, the skeletal and the ocular system. Interestingly, many cases of patients with Marfan syndrome and s...

Descripción completa

Detalles Bibliográficos
Autores principales: Dhakouani, S., Kammoun, R., Aissaoui, C., Karoui, M., Ellouz, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9567458/
http://dx.doi.org/10.1192/j.eurpsy.2022.1171
_version_ 1784809402032717824
author Dhakouani, S.
Kammoun, R.
Aissaoui, C.
Karoui, M.
Ellouz, F.
author_facet Dhakouani, S.
Kammoun, R.
Aissaoui, C.
Karoui, M.
Ellouz, F.
author_sort Dhakouani, S.
collection PubMed
description INTRODUCTION: Marfan syndrome is an autosomal dominant systemic disorder with connective tissue defects in multiple organ systems. Cardinal manifestations of this syndrome involve the cardiovascular, the skeletal and the ocular system. Interestingly, many cases of patients with Marfan syndrome and schizophrenia have been reported. OBJECTIVES: Discuss the etiological link between Marfan syndrome and schizophrenia METHODS: Presentation of a clinical case illustrating the comorbidity between schizophrenia and marfan syndrome. A search was conducted in PubMed database using the terms : schizophrenia AND Marfan syndrome. RESULTS: Ms JW a 36-year- old single women, she had schizophrenia since the age of 20 years, she was hospitalized in our service for psychotic relapse in a context of treatment discontinuation. She had a personal history of persistence of the ductus arteriosus for which she had been operated during her childhood, a scoliosis operated and multiple pathological fractures. On mental status examination, she was distressed and hallucinated, She had disorganized thought processes and a paranoid delirium. On physical examination, she had features suggestive of Marfan syndrome such as crowded teeth, a high arched palate, arachnodactyly , hyperlaxity and a high myopia. We don’t dispose genetic evaluation for marfan syndrom because of the nonavaibility of facilities to perform genetic analysis. Several studies have indicated that psychiatric symptoms might be part of the clinical profiles of marfan syndrom. However, their relationship and underlying pathogenesis are not easily clarified. CONCLUSIONS: Co-occurrence of marfan syndrom and schizophrenia might be explained by some shared etiological pathways between both disorders. DISCLOSURE: No significant relationships.
format Online
Article
Text
id pubmed-9567458
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Cambridge University Press
record_format MEDLINE/PubMed
spelling pubmed-95674582022-10-17 Marfan syndrome and schizophrenia : a case report and literature review Dhakouani, S. Kammoun, R. Aissaoui, C. Karoui, M. Ellouz, F. Eur Psychiatry Abstract INTRODUCTION: Marfan syndrome is an autosomal dominant systemic disorder with connective tissue defects in multiple organ systems. Cardinal manifestations of this syndrome involve the cardiovascular, the skeletal and the ocular system. Interestingly, many cases of patients with Marfan syndrome and schizophrenia have been reported. OBJECTIVES: Discuss the etiological link between Marfan syndrome and schizophrenia METHODS: Presentation of a clinical case illustrating the comorbidity between schizophrenia and marfan syndrome. A search was conducted in PubMed database using the terms : schizophrenia AND Marfan syndrome. RESULTS: Ms JW a 36-year- old single women, she had schizophrenia since the age of 20 years, she was hospitalized in our service for psychotic relapse in a context of treatment discontinuation. She had a personal history of persistence of the ductus arteriosus for which she had been operated during her childhood, a scoliosis operated and multiple pathological fractures. On mental status examination, she was distressed and hallucinated, She had disorganized thought processes and a paranoid delirium. On physical examination, she had features suggestive of Marfan syndrome such as crowded teeth, a high arched palate, arachnodactyly , hyperlaxity and a high myopia. We don’t dispose genetic evaluation for marfan syndrom because of the nonavaibility of facilities to perform genetic analysis. Several studies have indicated that psychiatric symptoms might be part of the clinical profiles of marfan syndrom. However, their relationship and underlying pathogenesis are not easily clarified. CONCLUSIONS: Co-occurrence of marfan syndrom and schizophrenia might be explained by some shared etiological pathways between both disorders. DISCLOSURE: No significant relationships. Cambridge University Press 2022-09-01 /pmc/articles/PMC9567458/ http://dx.doi.org/10.1192/j.eurpsy.2022.1171 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Dhakouani, S.
Kammoun, R.
Aissaoui, C.
Karoui, M.
Ellouz, F.
Marfan syndrome and schizophrenia : a case report and literature review
title Marfan syndrome and schizophrenia : a case report and literature review
title_full Marfan syndrome and schizophrenia : a case report and literature review
title_fullStr Marfan syndrome and schizophrenia : a case report and literature review
title_full_unstemmed Marfan syndrome and schizophrenia : a case report and literature review
title_short Marfan syndrome and schizophrenia : a case report and literature review
title_sort marfan syndrome and schizophrenia : a case report and literature review
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9567458/
http://dx.doi.org/10.1192/j.eurpsy.2022.1171
work_keys_str_mv AT dhakouanis marfansyndromeandschizophreniaacasereportandliteraturereview
AT kammounr marfansyndromeandschizophreniaacasereportandliteraturereview
AT aissaouic marfansyndromeandschizophreniaacasereportandliteraturereview
AT karouim marfansyndromeandschizophreniaacasereportandliteraturereview
AT ellouzf marfansyndromeandschizophreniaacasereportandliteraturereview