The Ehlers–Danlos syndromes
Sign Up to like & getrecommendations! Published in 2020 at "Nature Reviews Disease Primers"
DOI: 10.1038/s41572-020-0194-9
Abstract: The Ehlers–Danlos syndromes (EDS) are a heterogeneous group of hereditary disorders of connective tissue, with common features including joint hypermobility, soft and hyperextensible skin, abnormal wound healing and easy bruising. Fourteen different types of EDS… read more here.
Keywords: medicine; ehlers danlos; connective tissue; danlos syndromes ... See more keywords
Skin biopsy reveals generalized small fibre neuropathy in hypermobile Ehlers–Danlos syndromes
Sign Up to like & getrecommendations! Published in 2022 at "European Journal of Neurology"
DOI: 10.1111/ene.15649
Abstract: Ehlers–Danlos syndromes are hereditary disorders of connective tissue that are characterized by joint hypermobility, skin hyperextensibility and tissue fragility. The most common subtype is the hypermobile type. In addition to symptoms of small fibre neuropathy… read more here.
Keywords: fibre neuropathy; small fibre; danlos syndromes; hypermobile ehlers ... See more keywords
Multidisciplinary chronic pain management strategies in patients with Ehlers-Danlos syndromes.
Sign Up to like & getrecommendations! Published in 2022 at "Pain management"
DOI: 10.2217/pmt-2022-0050
Abstract: Ehlers-Danlos syndromes (EDS) are a group of disorders characterized by abnormal connective tissue affecting several organ systems. Patients with the hypermobile type of EDS (hEDS) commonly experience chronic pain which can present as musculoskeletal pain,… read more here.
Keywords: pain management; danlos syndromes; chronic pain; pain ... See more keywords
Ehlers-Danlos syndromes and their manifestations in the visual system
Sign Up to like & getrecommendations! Published in 2022 at "Frontiers in Medicine"
DOI: 10.3389/fmed.2022.996458
Abstract: Ehlers-Danlos syndrome (EDS) is a rare, genetically variable, heterogenous group of (currently recognized) thirteen connective tissue disorders characterized by skin hyperextensibility, tissue fragility, and generalized joint hypermobility. In addition to these commonly recognized phenotypes, recent… read more here.
Keywords: syndromes manifestations; danlos syndromes; ehlers danlos; visual system ... See more keywords
Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes
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DOI: 10.3390/genes10080609
Abstract: The Ehlers‒Danlos syndromes (EDS) constitute a heterogenous group of connective tissue disorders characterized by joint hypermobility, skin abnormalities, and vascular fragility. The latest nosology recognizes 13 types caused by pathogenic variants in genes encoding collagens… read more here.
Keywords: pathogenesis; danlos syndromes; ehlers danlos; ceds veds ... See more keywords
The Ehlers–Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism
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DOI: 10.3390/genes13020265
Abstract: The Ehlers–Danlos syndromes are a group of multisystemic heritable connective tissue disorders with clinical presentations that range from multiple congenital malformations, over adolescent-onset debilitating or even life-threatening complications of connective tissue fragility, to mild conditions… read more here.
Keywords: inborn errors; errors metabolism; fragility; danlos syndromes ... See more keywords
The Relationship between Autism and Ehlers-Danlos Syndromes/Hypermobility Spectrum Disorders
Sign Up to like & getrecommendations! Published in 2020 at "Journal of Personalized Medicine"
DOI: 10.3390/jpm10040260
Abstract: Considerable interest has arisen concerning the relationship between hereditary connective tissue disorders such as the Ehlers-Danlos syndromes (EDS)/hypermobility spectrum disorders (HSD) and autism, both in terms of their comorbidity as well as co-occurrence within the… read more here.
Keywords: hypermobility spectrum; spectrum disorders; autism; danlos syndromes ... See more keywords