Hypermobile type Ehlers‐Danlos syndrome associated with hypogammaglobulinemia and fibromyalgia: A case‐based review on new classification, diagnosis, and multidisciplinary management

Hypermobile type Ehlers‐Danlos syndrome (hEDS) is an underdiagnosed connective tissue disorder characterized by generalized joint hypermobility, chronic fatigue, widespread joints pain, and impaired quality of life. Here, we reported the first hEDS complicated by hypogammaglobulinemia. New insights...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Wei, Windsor, Kevin, Jones, Richard, Taunton, David Oscar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452458/
https://www.ncbi.nlm.nih.gov/pubmed/30997063
http://dx.doi.org/10.1002/ccr3.2070
_version_ 1783409292634750976
author Zhang, Wei
Windsor, Kevin
Jones, Richard
Taunton, David Oscar
author_facet Zhang, Wei
Windsor, Kevin
Jones, Richard
Taunton, David Oscar
author_sort Zhang, Wei
collection PubMed
description Hypermobile type Ehlers‐Danlos syndrome (hEDS) is an underdiagnosed connective tissue disorder characterized by generalized joint hypermobility, chronic fatigue, widespread joints pain, and impaired quality of life. Here, we reported the first hEDS complicated by hypogammaglobulinemia. New insights into classification, diagnosis, and proper management of hEDS are also reviewed.
format Online
Article
Text
id pubmed-6452458
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-64524582019-04-17 Hypermobile type Ehlers‐Danlos syndrome associated with hypogammaglobulinemia and fibromyalgia: A case‐based review on new classification, diagnosis, and multidisciplinary management Zhang, Wei Windsor, Kevin Jones, Richard Taunton, David Oscar Clin Case Rep Case Reports Hypermobile type Ehlers‐Danlos syndrome (hEDS) is an underdiagnosed connective tissue disorder characterized by generalized joint hypermobility, chronic fatigue, widespread joints pain, and impaired quality of life. Here, we reported the first hEDS complicated by hypogammaglobulinemia. New insights into classification, diagnosis, and proper management of hEDS are also reviewed. John Wiley and Sons Inc. 2019-02-19 /pmc/articles/PMC6452458/ /pubmed/30997063 http://dx.doi.org/10.1002/ccr3.2070 Text en © 2019 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Zhang, Wei
Windsor, Kevin
Jones, Richard
Taunton, David Oscar
Hypermobile type Ehlers‐Danlos syndrome associated with hypogammaglobulinemia and fibromyalgia: A case‐based review on new classification, diagnosis, and multidisciplinary management
title Hypermobile type Ehlers‐Danlos syndrome associated with hypogammaglobulinemia and fibromyalgia: A case‐based review on new classification, diagnosis, and multidisciplinary management
title_full Hypermobile type Ehlers‐Danlos syndrome associated with hypogammaglobulinemia and fibromyalgia: A case‐based review on new classification, diagnosis, and multidisciplinary management
title_fullStr Hypermobile type Ehlers‐Danlos syndrome associated with hypogammaglobulinemia and fibromyalgia: A case‐based review on new classification, diagnosis, and multidisciplinary management
title_full_unstemmed Hypermobile type Ehlers‐Danlos syndrome associated with hypogammaglobulinemia and fibromyalgia: A case‐based review on new classification, diagnosis, and multidisciplinary management
title_short Hypermobile type Ehlers‐Danlos syndrome associated with hypogammaglobulinemia and fibromyalgia: A case‐based review on new classification, diagnosis, and multidisciplinary management
title_sort hypermobile type ehlers‐danlos syndrome associated with hypogammaglobulinemia and fibromyalgia: a case‐based review on new classification, diagnosis, and multidisciplinary management
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452458/
https://www.ncbi.nlm.nih.gov/pubmed/30997063
http://dx.doi.org/10.1002/ccr3.2070
work_keys_str_mv AT zhangwei hypermobiletypeehlersdanlossyndromeassociatedwithhypogammaglobulinemiaandfibromyalgiaacasebasedreviewonnewclassificationdiagnosisandmultidisciplinarymanagement
AT windsorkevin hypermobiletypeehlersdanlossyndromeassociatedwithhypogammaglobulinemiaandfibromyalgiaacasebasedreviewonnewclassificationdiagnosisandmultidisciplinarymanagement
AT jonesrichard hypermobiletypeehlersdanlossyndromeassociatedwithhypogammaglobulinemiaandfibromyalgiaacasebasedreviewonnewclassificationdiagnosisandmultidisciplinarymanagement
AT tauntondavidoscar hypermobiletypeehlersdanlossyndromeassociatedwithhypogammaglobulinemiaandfibromyalgiaacasebasedreviewonnewclassificationdiagnosisandmultidisciplinarymanagement

Ejemplares similares