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About 3,182 results

ALLMedicine™ Ehlers-Danlos Syndrome Center

Research & Reviews  1,553 results

Clinical and genetic analysis of classical Ehlers-Danlos syndrome patient caused by syn...
https://doi.org/10.1002/mgg3.1632
Molecular Genetics & Genomic Medicine; Ma N, Zhu Z et. al.

Apr 9th, 2021 - Classical Ehlers-Danlos syndrome (cEDS) is a heterogeneous connective tissue disorder that mainly results from the germline mutation of COL5A1 and COL5A2. The majority of the COL5A2 mutations reported to date represent structural mutations, includ...

Finger orthoses for management of joint hypermobility disorders: Relative effects on ha...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7978036
Prosthetics and Orthotics International; Jensen AM, Andersen JQ et. al.

Apr 9th, 2021 - Joint hypermobility refers to joints that move beyond their normal limits. Individuals with hypermobility of the fingers experience difficulties in activities of daily living. Finger orthoses are available for managing hypermobility of the fingers...

Aortic rupture by an acute dissection of the thoracoabdominal aorta in a 12-year-old boy.
https://doi.org/10.1016/j.avsg.2021.03.025
Annals of Vascular Surgery; Conejero AM, Horcajo RR et. al.

Apr 9th, 2021 - Aortic dissection is exceptional in children. When they are affected, many clinical conditions as Marfan syndrome or Ehlers-Danlos syndrome are usually involved, but up to 22% have no associated background. Its high morbidity and low incidence in ...

Subtle differences in autonomic symptoms in people diagnosed with hypermobile Ehlers-Da...
https://doi.org/10.1002/ajmg.a.62197
American Journal of Medical Genetics. Part A; Martinez KL, Mauss C et. al.

Apr 7th, 2021 - The hypermobile Ehlers-Danlos syndrome (hEDS) GENE study is a multicenter, cohort study with the goal to identify genes associated with hypermobile EDS. Of the 148 people enrolled in the hEDS GENE study, 98 meet the 2017 hEDS criteria, 27 have a h...

Shoulder Arthroplasty is a Viable Option in Patients with Ehlers-Danlos Syndrome.
https://doi.org/10.1016/j.jse.2021.03.146
Journal of Shoulder and Elbow Surgery; Rogers T, Werthel JD et. al.

Apr 3rd, 2021 - Patients with Ehlers-Danlos Syndrome (EDS) have high rates of shoulder instability, which place them at increased risk for instability-related arthropathy. Many studies have assessed outcomes for both primary and revision shoulder instability proc...

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Clinicaltrials.gov  1,587 results

Clinical and genetic analysis of classical Ehlers-Danlos syndrome patient caused by syn...
https://doi.org/10.1002/mgg3.1632
Molecular Genetics & Genomic Medicine; Ma N, Zhu Z et. al.

Apr 9th, 2021 - Classical Ehlers-Danlos syndrome (cEDS) is a heterogeneous connective tissue disorder that mainly results from the germline mutation of COL5A1 and COL5A2. The majority of the COL5A2 mutations reported to date represent structural mutations, includ...

Finger orthoses for management of joint hypermobility disorders: Relative effects on ha...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7978036
Prosthetics and Orthotics International; Jensen AM, Andersen JQ et. al.

Apr 9th, 2021 - Joint hypermobility refers to joints that move beyond their normal limits. Individuals with hypermobility of the fingers experience difficulties in activities of daily living. Finger orthoses are available for managing hypermobility of the fingers...

Aortic rupture by an acute dissection of the thoracoabdominal aorta in a 12-year-old boy.
https://doi.org/10.1016/j.avsg.2021.03.025
Annals of Vascular Surgery; Conejero AM, Horcajo RR et. al.

Apr 9th, 2021 - Aortic dissection is exceptional in children. When they are affected, many clinical conditions as Marfan syndrome or Ehlers-Danlos syndrome are usually involved, but up to 22% have no associated background. Its high morbidity and low incidence in ...

Subtle differences in autonomic symptoms in people diagnosed with hypermobile Ehlers-Da...
https://doi.org/10.1002/ajmg.a.62197
American Journal of Medical Genetics. Part A; Martinez KL, Mauss C et. al.

Apr 7th, 2021 - The hypermobile Ehlers-Danlos syndrome (hEDS) GENE study is a multicenter, cohort study with the goal to identify genes associated with hypermobile EDS. Of the 148 people enrolled in the hEDS GENE study, 98 meet the 2017 hEDS criteria, 27 have a h...

Shoulder Arthroplasty is a Viable Option in Patients with Ehlers-Danlos Syndrome.
https://doi.org/10.1016/j.jse.2021.03.146
Journal of Shoulder and Elbow Surgery; Rogers T, Werthel JD et. al.

Apr 3rd, 2021 - Patients with Ehlers-Danlos Syndrome (EDS) have high rates of shoulder instability, which place them at increased risk for instability-related arthropathy. Many studies have assessed outcomes for both primary and revision shoulder instability proc...

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News  29 results

What You Should Know About Ehlers-Danlos Syndrome
https://www.medscape.com/viewarticle/947306

Mar 14th, 2021 - Ehlers-Danlos syndrome (EDS) refers to a heterogeneous group of heritable disorders of connective tissue resulting in tissue fragility, skin hyperextensibility, and joint hypermobility. The true prevalence is unknown but is estimated at 1 in 5000....

Ehlers-Danlos Syndrome Associated With Various Complications in Hospitalized Patients
https://www.medscape.com/viewarticle/944006

Jan 12th, 2021 - Hospitalized patients with Ehlers-Danlos syndrome (EDS) are more likely to have gastrointestinal, cardiovascular, autonomic, and allergic disorders than are hospitalized patients who do not have EDS, according to a new study of hospital outcomes i...

FDA declines to approve Acer Therapeutics' rare genetic disorder treatment
https://www.reuters.com/article/us-acer-therape-fda/fda-declines-to-approve-acer-therapeutics-rare-genetic-disorder-treatment-idUSKCN1TQ1K9

Jun 25th, 2019 - (Reuters) - Acer Therapeutics Inc said on Tuesday the U.S. Food and Drug Administration declined to approve its treatment for a severe, rare genetic disorder that can cause blood vessels to fatally rupture, sending its shares plunging as much as 7...

Multiple Eruptive Syringomas on the Penis
https://www.mdedge.com/dermatology/article/201251/pediatrics?channel=44
Weihuang Vivian Ning, MD, Sameer Bashey, MD et. al.

May 20th, 2019 - To the Editor: Syringomas are small, benign, asymptomatic eccrine or apocrine tumors that present as multiple discrete flesh-colored papules. They are more common in females than males.

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Patient Education  13 results see all →