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Ectodermal disturbance in development shared by anorexia and schizophrenia may reflect neurodevelopmental abnormalities
Minor physical abnormalities (MPA) are subtle dysmorphic features of bodily structures that have little or no impact on function. Most MPA develop during the first gestational trimester and are considered as important indicators of neuroectodermal deficiencies emerging during early brain development...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553323/ https://www.ncbi.nlm.nih.gov/pubmed/34510800 http://dx.doi.org/10.1002/brb3.2281 |
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author | Remberk, Barbara Niwiński, Piotr Brzóska‐Konkol, Ewa Borowska, Anna Papasz‐Siemieniuk, Anna Brągoszewska, Joanna Bażyńska, Anna Katarzyna Szostakiewicz, Łukasz Herman, Anna |
author_facet | Remberk, Barbara Niwiński, Piotr Brzóska‐Konkol, Ewa Borowska, Anna Papasz‐Siemieniuk, Anna Brągoszewska, Joanna Bażyńska, Anna Katarzyna Szostakiewicz, Łukasz Herman, Anna |
author_sort | Remberk, Barbara |
collection | PubMed |
description | Minor physical abnormalities (MPA) are subtle dysmorphic features of bodily structures that have little or no impact on function. Most MPA develop during the first gestational trimester and are considered as important indicators of neuroectodermal deficiencies emerging during early brain development. A higher frequency of MPA was confirmed in schizophrenia patients and their relatives, when compared to controls. These findings are consistent with the neurodevelopmental model of schizophrenia. A neurodevelopmental component amongst other risk factors has also been recently proposed for anorexia nervosa (AN). The current study aimed to assess MPA frequency in adolescent inpatients with either schizophrenia spectrum disorders (SSD) or AN as compared to healthy controls (HC). The Waldrop Scale was used for assessing MPA. The mean MPA total score and mean head subscore was significantly higher in both test groups than in HC. There were no statistically significant differences between SSD and AN groups. The MPA profile (not frequency) was similar in all three groups. This finding is consistent both with widely acknowledged neurodevelopmental schizophrenia hypothesis as well as with more recent neurodevelopmental model of AN. Nevertheless, the findings should not be overgeneralized and further studies are warranted. |
format | Online Article Text |
id | pubmed-8553323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85533232021-11-04 Ectodermal disturbance in development shared by anorexia and schizophrenia may reflect neurodevelopmental abnormalities Remberk, Barbara Niwiński, Piotr Brzóska‐Konkol, Ewa Borowska, Anna Papasz‐Siemieniuk, Anna Brągoszewska, Joanna Bażyńska, Anna Katarzyna Szostakiewicz, Łukasz Herman, Anna Brain Behav Original Research Minor physical abnormalities (MPA) are subtle dysmorphic features of bodily structures that have little or no impact on function. Most MPA develop during the first gestational trimester and are considered as important indicators of neuroectodermal deficiencies emerging during early brain development. A higher frequency of MPA was confirmed in schizophrenia patients and their relatives, when compared to controls. These findings are consistent with the neurodevelopmental model of schizophrenia. A neurodevelopmental component amongst other risk factors has also been recently proposed for anorexia nervosa (AN). The current study aimed to assess MPA frequency in adolescent inpatients with either schizophrenia spectrum disorders (SSD) or AN as compared to healthy controls (HC). The Waldrop Scale was used for assessing MPA. The mean MPA total score and mean head subscore was significantly higher in both test groups than in HC. There were no statistically significant differences between SSD and AN groups. The MPA profile (not frequency) was similar in all three groups. This finding is consistent both with widely acknowledged neurodevelopmental schizophrenia hypothesis as well as with more recent neurodevelopmental model of AN. Nevertheless, the findings should not be overgeneralized and further studies are warranted. John Wiley and Sons Inc. 2021-09-12 /pmc/articles/PMC8553323/ /pubmed/34510800 http://dx.doi.org/10.1002/brb3.2281 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Remberk, Barbara Niwiński, Piotr Brzóska‐Konkol, Ewa Borowska, Anna Papasz‐Siemieniuk, Anna Brągoszewska, Joanna Bażyńska, Anna Katarzyna Szostakiewicz, Łukasz Herman, Anna Ectodermal disturbance in development shared by anorexia and schizophrenia may reflect neurodevelopmental abnormalities |
title | Ectodermal disturbance in development shared by anorexia and schizophrenia may reflect neurodevelopmental abnormalities |
title_full | Ectodermal disturbance in development shared by anorexia and schizophrenia may reflect neurodevelopmental abnormalities |
title_fullStr | Ectodermal disturbance in development shared by anorexia and schizophrenia may reflect neurodevelopmental abnormalities |
title_full_unstemmed | Ectodermal disturbance in development shared by anorexia and schizophrenia may reflect neurodevelopmental abnormalities |
title_short | Ectodermal disturbance in development shared by anorexia and schizophrenia may reflect neurodevelopmental abnormalities |
title_sort | ectodermal disturbance in development shared by anorexia and schizophrenia may reflect neurodevelopmental abnormalities |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553323/ https://www.ncbi.nlm.nih.gov/pubmed/34510800 http://dx.doi.org/10.1002/brb3.2281 |
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