The discussions reflect curiosity and support for the updated classification, with comments such as 'Next year when the Ehlers-Danlos Society initiative Road to 2026 gather' indicating anticipation for future revisions, and references to specific mutations like '50% have COL5A1 or COL5A2', highlighting detailed engagement with the research. The tone varies from informative to slightly critical, emphasizing the evolving understanding and ongoing debates within the community.
AgreementModerate agreement
Most discussions acknowledge and support the significance of the updated classification, with some referencing the ongoing review process and the importance of genetic findings.
InterestHigh interest
Posts demonstrate a high level of curiosity and engagement, discussing specifics of the classification, genetic mutations, and diagnostic criteria.
EngagementModerate engagement
Participants engage deeply by sharing links, clarifications, and references to research, indicating thoughtful interactions.
ImpactModerate impact
The conversations suggest the publication influences the community, with references to upcoming reviews and the need for awareness around diagnosis and classification tools.
Abstract in brief
* Recent advances have revealed new EDS subtypes and genetic mutations, prompting the International EDS Consortium to propose a revised classification that recognizes 13 subtypes along with specific clinical diagnosis criteria.
* The revised classification aims to address the genetic and clinical complexity of EDS, emphasizing the importance of genetic testing for most subtypes and improving distinctions between hypermobile EDS and other related disorders.
REFERÊNCIA:
MALFAIT, Fransiska et al. The 2017 international classification of the Ehlers–Danlos syndromes. In: American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 2017. p. 8-26.
May 21, 2023 · 2 likes · 4,504 followersView post →
PJ
Pierre Vabres (moi/je)
@pierrevabres · X
@dame_vae Hélas non.
La définition du syndrome d'Ehlers-Danlos hypermobile est encore incertaine. Ce diagnostic est souvent porté par excès.
Pas de test génétique pour cette forme d'EDS. Les critères cliniques proposés ont été accompagnés d'une mise en garde.
https://t.co/8sBE7C6iYl https://t.co/1gjMVx6JCH
Jan 19, 2020 · 2 likes · 2,739 followersView post →
D
dheurtevent
@dheurtevent1 · X
@tay_loup Où as-tu lu ça ? La cause est un série de mutation génétique, 13 soustype reconnus internationalement en 2017.
https://t.co/UP9pgbUeKV
50% ont un mutation COL5A1 ou COL5A2
https://t.co/d1rtmqiu0C
Beaucoup de bullshit dans la littérature SED, dérive de médecine intégrative, etc.
@lynnery38 @BluesteinLinda But it's going to. Next year when the Ehlers-Danlos Society initiative Road to 2026 gather they will review the 2017 International Classification of the Ehlers-Danlos syndromes. It's just a matter of time now.
An overview of the Ehlers-Danlos syndromes, their classification, clinical presentation, diagnostic criteria, and recent advances in genetics and subtype distinctions.
This video explores the relationship between hypermobility and scoliosis, offering insights into managing joint pain and injury risks with safe, targeted exercises. It includes a hypermobility assessment test and shares…
@lynnery38 @BluesteinLinda But it's going to. Next year when the Ehlers-Danlos Society initiative Road to 2026 gather they will review the 2017 International Classification of the Ehlers-Danlos syndromes. It's just a matter of time now.
Don’t forget to diagnose your newly turned 50 patients with hypermobile Ehlers-Danlos syndrome!
The work by Malfait et al. is surely well done…
https://t.co/9OqOEtuNtL
@PutAimovigOnNHS @davidtuller1 Thanks for your comments but these are the 2017 hEDS criteria:
https://t.co/GzjSobqGx0
The skin properties you describe are suggestive of classical and classical-like EDS, not hEDS.
Oct 17, 2024 · 1 like · 4,638 followersView post →
M
⚣︎ Melinda
@fitocanibalismo · X
RT @giulliarruda: REFERÊNCIA:
MALFAIT, Fransiska et al. The 2017 international classification of the Ehlers–Danlos syndromes. In: American…
REFERÊNCIA:
MALFAIT, Fransiska et al. The 2017 international classification of the Ehlers–Danlos syndromes. In: American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 2017. p. 8-26.
Image Credit: The image above is taken from the research paper, The 2017 international classification of the Ehlers–Danlos syndromes: https://t.co/yBat4xusbB
Apr 2, 2024 · 1 like · 18,358 followersView post →
닭
닭스무살
@9lqq6 · X
The 2017 International Classification of the Ehlers-Danlos syndromes replaced previous terms ... with hypermobile EDS and introduced the term hypermobility spectrum disorders for patients not meeting diagnostic criteria for hypermobile EDS.
https://t.co/8T0UFVd7Pm
@cinaramdoss @danizinhawnx @reumalho só umas correções: Teste de Beighton é uma avaliação, não um sistema, e não é só para SED; e nosologia é o estudo dos sintomas, que toda condição tem sua própria nosologia
Aqui a de SED
https://t.co/3va8ZlrlRd
@tay_loup Où as-tu lu ça ? La cause est un série de mutation génétique, 13 soustype reconnus internationalement en 2017.
https://t.co/UP9pgbUeKV
50% ont un mutation COL5A1 ou COL5A2
https://t.co/d1rtmqiu0C
Beaucoup de bullshit dans la littérature SED, dérive de médecine intégrative, etc.
@hiimjakekthx Actually, I found it pretty easily. Here’s a link, and her name highlighted.
Those involved in the community at the time will remember her swearing up and down that she and the Society had no part in writing them, which was horseshit.
https://t.co/71RG1Qsoy4 https://t.co/6NGM39HZ4v
Dec 23, 2022 · 1 like · 2,183 followersView post →
KB
Kelsey J.R.P. Byers
@plantpollinator · X
@philinidae If you want to take a look at the current diagnostic criteria, look at this paper:
https://t.co/Ut9oa53Rw2
actually the whole issue is very helpful if you can parse the science.
@raimeygallant @MomijiWolfMaple @UntoNuggan Mild hyper extensibility is one of the current criteria you could have as part of 2B https://t.co/CoROPVm58K
Comorbidities include sleep disturbance, fatigue, POTS, functional gastrointestinal disorders, dysautonomia, anxiety, & depression and are debilitating. Malfait F et al. Am J Med Genet C Semin Med Genet. March, 2017; 175(1):8-26. #HEDS @loosefacts
https://t.co/81PBnVexCc.
@chaotic_kat Ok, sorry, brain fog took over and I totally forgot to look for this! So sorry!
Here is one pic, scroll down the page for a shot of some scar pics. I believe this is the "cigarette paper" scarring https://t.co/4x4fYC5yjU
@dame_vae Hélas non.
La définition du syndrome d'Ehlers-Danlos hypermobile est encore incertaine. Ce diagnostic est souvent porté par excès.
Pas de test génétique pour cette forme d'EDS. Les critères cliniques proposés ont été accompagnés d'une mise en garde.
https://t.co/8sBE7C6iYl https://t.co/1gjMVx6JCH
Jan 19, 2020 · 2 likes · 2,739 followersView post →
... 10.1002/ajmg.c. 31552... And here's the official EDS Society paper which includes a VERRRY indepth description of the 'how to' of hte hEDS diagnostic ...
... 10.1002/ajmg.c.31552 ). This is unusual, as usually we consider 'recessive' to mean inconsequential if you have 1 good / 1 bad copy. But, TNXB needs 2 good ...
Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):8-26. doi: 10.1002/ajmg.c.31552. Citation on PubMed; Schalkwijk J, Zweers MC, Steijlen PM, Dean WB, Taylor ...
Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):8-26. doi: 10.1002/ajmg.c.31552. Citation on PubMed; Murray ML, Yang M, Fauth C, Byers PH. FKBP14-related ...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 175(1), 212–219. https://doi. org/10.1002/ajmg.c.31552. TikTok · Becca Jeremiah.
doi: 10.1002/ajmg.c.31552. Citation on PubMed (https://pub med.ncbi.nlm.nih.gov/28306229). • Schalkwijk J, Zweers MC, Steijlen PM, Dean WB, Taylor G, van ...
... paper also goes over other features and other subtypes. https://onlinelibrary.wiley.com/doi/10.1002/ajmg.c.31552 · Acrobatic_Block4226. OP • 5d ...