Results 21 to 30 of about 24,908 (251)

Multiple odontogenic keratocysts in Ehlers–Danlos syndrome: a rare case report

open access: yesBMC Oral Health, 2021
Background An odontogenic keratocyst is a lesion characterized by aggressive and infiltrative growth. The lesion is characterized by the existence of satellite microcysts (microtumours) and frequent recurrence (up to 30%).
Anna Starzyńska   +6 more
doaj   +1 more source

Anesthetic management of a patient with musculocontractural Ehlers-Danlos syndrome undergoing scoliosis surgery

open access: yesJA Clinical Reports, 2020
Background Musculocontractural Ehlers-Danlos syndrome is a new and rare subtype of Ehlers-Danlos syndrome in which anesthetic considerations for airway and respiratory management, prevention of skin injuries and joint dislocations, and hemostatic ...
Ryo Wakabayashi   +6 more
doaj   +1 more source

Association Between Joint Hypermobility Syndrome and Developmental Coordination Disorder – A Review. [PDF]

open access: yes, 2012
Introduction: The term joint hypermobility syndrome (JHS) was adopted after clinicians became aware of the myriad of symptoms associated with this multisystemic condition.
Clark, Carol J., Khattab, Ahmed D.
core   +1 more source

Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndrome [PDF]

open access: yes, 2013
Background: Whereas mutations affecting the helical domain of type I procollagen classically cause Osteogenesis Imperfecta (OI), helical mutations near the amino (N)-proteinase cleavage site have been suggested to result in a mixed OI/Ehlers-Danlos ...
De Paepe, Anne   +9 more
core   +2 more sources

Psychological interventions for individuals with Ehlers-Danlos syndrome and hypermobility spectrum disorder: a scoping review

open access: yesOrphanet Journal of Rare Diseases, 2023
Purpose To identify the nature and extent of the evidence on psychological interventions among individuals with Ehlers-Danlos Syndrome (EDS) and Hypermobility Spectrum Disorder (HSD).
Jessica Z. Song   +9 more
doaj   +1 more source

Higher fracture prevalence and smaller bone size in patients with hEDS/HSD-a prospective cohort study

open access: yes, 2020
Increased fracture risk in patients with Ehlers-Danlos syndromes has been reported, but the reasons for it are incompletely understood. We aimed to investigate possible determinants of this increased risk and found that hEDS/HSD patients present with a ...
Banica, Thiberiu   +9 more
core   +1 more source

Clinical periodontal diagnosis

open access: yesPeriodontology 2000, EarlyView., 2023
Abstract Periodontal diseases include pathological conditions elicited by the presence of bacterial biofilms leading to a host response. In the diagnostic process, clinical signs such as bleeding on probing, development of periodontal pockets and gingival recessions, furcation involvement and presence of radiographic bone loss should be assessed prior ...
Giovanni E. Salvi   +5 more
wiley   +1 more source

Updates in Clinical and Genetics Aspects of Hypermobile Ehlers Danlos Syndrome

open access: yesBalkan Medical Journal, 2019
Efforts on recognition, diagnosis, and management of the presumed, most common connective tissue disorder hypermobile Ehlers-Danlos syndrome have been an ongoing challenge, even decades after the description of this condition.
Irman Forghani
doaj   +1 more source

Ruptured ulnar artery aneurysm in vascular Ehlers-Danlos syndrome

open access: yesJournal of Vascular Surgery Cases and Innovative Techniques, 2020
Vascular Ehlers-Danlos syndrome (vEDS), also known as type IV Ehlers-Danlos syndrome, is a rare inherited connective tissue disease that affects 1 in 50,000 to 250,000 individuals.
Ryan Howard, MD, Nicholas Osborne, MD
doaj   +1 more source

Adults with Loeys-Dietz syndrome and vascular Ehlers-Danlos syndrome: A cross-sectional study of life satisfaction

open access: yesJournal of Rehabilitation Medicine, 2021
Objective: To explore life satisfaction among adults with Loeys-Dietz and those with vascular Ehlers-Danlos syndrome. Design: Postal survey in 2018. Participants and methods: Persons with molecularly verified Loeys-Dietz syndrome or vascular Ehlers ...
Heidi Johansen   +3 more
doaj   +1 more source

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