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A rare case of acrogeria, Gottron type with borderline personality disorder

Acrogeria is a rare disorder that is characterized by premature aging of the distal extremities. It was first described by Gottron in 1941. Only about 50 cases have yet been reported worldwide. It is diagnosed clinically, and patients have a normal life expectancy. The disorder is seen from birth an...

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Autores principales: Sawant, Neena, Mehta, Anjali, Chaturvedi, Hemashri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638570/
https://www.ncbi.nlm.nih.gov/pubmed/36353018
http://dx.doi.org/10.4103/jfmpc.jfmpc_40_22
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author Sawant, Neena
Mehta, Anjali
Chaturvedi, Hemashri
author_facet Sawant, Neena
Mehta, Anjali
Chaturvedi, Hemashri
author_sort Sawant, Neena
collection PubMed
description Acrogeria is a rare disorder that is characterized by premature aging of the distal extremities. It was first described by Gottron in 1941. Only about 50 cases have yet been reported worldwide. It is diagnosed clinically, and patients have a normal life expectancy. The disorder is seen from birth and could have an autosomal dominant or recessive inheritance. The classic features include a characteristic pinched face, thin lips, fine hair, skeletal defects, and thin, taut parchment-like skin of the extremities. We describe a case of Acrogeria, Gottron type, who also had a borderline personality disorder. However, there is very little information on the prevalence of psychopathology in patients having syndromes of premature aging.
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spelling pubmed-96385702022-11-08 A rare case of acrogeria, Gottron type with borderline personality disorder Sawant, Neena Mehta, Anjali Chaturvedi, Hemashri J Family Med Prim Care Case Report Acrogeria is a rare disorder that is characterized by premature aging of the distal extremities. It was first described by Gottron in 1941. Only about 50 cases have yet been reported worldwide. It is diagnosed clinically, and patients have a normal life expectancy. The disorder is seen from birth and could have an autosomal dominant or recessive inheritance. The classic features include a characteristic pinched face, thin lips, fine hair, skeletal defects, and thin, taut parchment-like skin of the extremities. We describe a case of Acrogeria, Gottron type, who also had a borderline personality disorder. However, there is very little information on the prevalence of psychopathology in patients having syndromes of premature aging. Wolters Kluwer - Medknow 2022-08 2022-08-30 /pmc/articles/PMC9638570/ /pubmed/36353018 http://dx.doi.org/10.4103/jfmpc.jfmpc_40_22 Text en Copyright: © 2022 Journal of Family Medicine and Primary Care https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Sawant, Neena
Mehta, Anjali
Chaturvedi, Hemashri
A rare case of acrogeria, Gottron type with borderline personality disorder
title A rare case of acrogeria, Gottron type with borderline personality disorder
title_full A rare case of acrogeria, Gottron type with borderline personality disorder
title_fullStr A rare case of acrogeria, Gottron type with borderline personality disorder
title_full_unstemmed A rare case of acrogeria, Gottron type with borderline personality disorder
title_short A rare case of acrogeria, Gottron type with borderline personality disorder
title_sort rare case of acrogeria, gottron type with borderline personality disorder
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638570/
https://www.ncbi.nlm.nih.gov/pubmed/36353018
http://dx.doi.org/10.4103/jfmpc.jfmpc_40_22
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