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Mosaic Turner syndrome associated with schizophrenia

Turner syndrome is a sex-chromosome disorder; occurring in 1 in 2,500 female births. There are sporadic few case reports of concomitant Turner syndrome with schizophrenia worldwide. Most Turner females had a 45,X monosomy, whereas the majority of comorbidity between Turner syndrome and schizophrenia...

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Autores principales: Jung, Sook Young, Park, Joo Won, Kim, Dong Hyun, Jun, Yong Hoon, Lee, Jeong Seop, Lee, Ji Eun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Endocrinology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049549/
https://www.ncbi.nlm.nih.gov/pubmed/24926463
http://dx.doi.org/10.6065/apem.2014.19.1.42
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author Jung, Sook Young
Park, Joo Won
Kim, Dong Hyun
Jun, Yong Hoon
Lee, Jeong Seop
Lee, Ji Eun
author_facet Jung, Sook Young
Park, Joo Won
Kim, Dong Hyun
Jun, Yong Hoon
Lee, Jeong Seop
Lee, Ji Eun
author_sort Jung, Sook Young
collection PubMed
description Turner syndrome is a sex-chromosome disorder; occurring in 1 in 2,500 female births. There are sporadic few case reports of concomitant Turner syndrome with schizophrenia worldwide. Most Turner females had a 45,X monosomy, whereas the majority of comorbidity between Turner syndrome and schizophrenia had a mosaic karyotype (45,X/46,XX). We present a case of a 21-year-old woman with Turner syndrome, mosaic karyotype (45,X/46,XX), showing mental retardation, hypothyroidism, and schizophrenia. HOPA gene within Xq13 is related to mental retardation, hypothyroidism, and schizophrenia. Our case may be a potential clue which supports the hypothesis for involvement of genes on X chromosome in development of schizophrenia. Further studies including comorbid cases reports are need in order to discern the cause of schizophrenia in patients having Turner syndrome.
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spelling pubmed-40495492014-06-12 Mosaic Turner syndrome associated with schizophrenia Jung, Sook Young Park, Joo Won Kim, Dong Hyun Jun, Yong Hoon Lee, Jeong Seop Lee, Ji Eun Ann Pediatr Endocrinol Metab Case Report Turner syndrome is a sex-chromosome disorder; occurring in 1 in 2,500 female births. There are sporadic few case reports of concomitant Turner syndrome with schizophrenia worldwide. Most Turner females had a 45,X monosomy, whereas the majority of comorbidity between Turner syndrome and schizophrenia had a mosaic karyotype (45,X/46,XX). We present a case of a 21-year-old woman with Turner syndrome, mosaic karyotype (45,X/46,XX), showing mental retardation, hypothyroidism, and schizophrenia. HOPA gene within Xq13 is related to mental retardation, hypothyroidism, and schizophrenia. Our case may be a potential clue which supports the hypothesis for involvement of genes on X chromosome in development of schizophrenia. Further studies including comorbid cases reports are need in order to discern the cause of schizophrenia in patients having Turner syndrome. The Korean Society of Pediatric Endocrinology 2014-03 2014-03-31 /pmc/articles/PMC4049549/ /pubmed/24926463 http://dx.doi.org/10.6065/apem.2014.19.1.42 Text en © 2014 Annals of Pediatric Endocrinology & Metabolism http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jung, Sook Young
Park, Joo Won
Kim, Dong Hyun
Jun, Yong Hoon
Lee, Jeong Seop
Lee, Ji Eun
Mosaic Turner syndrome associated with schizophrenia
title Mosaic Turner syndrome associated with schizophrenia
title_full Mosaic Turner syndrome associated with schizophrenia
title_fullStr Mosaic Turner syndrome associated with schizophrenia
title_full_unstemmed Mosaic Turner syndrome associated with schizophrenia
title_short Mosaic Turner syndrome associated with schizophrenia
title_sort mosaic turner syndrome associated with schizophrenia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049549/
https://www.ncbi.nlm.nih.gov/pubmed/24926463
http://dx.doi.org/10.6065/apem.2014.19.1.42
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