Results 21 to 30 of about 1,170,712 (223)

Craniofacial Morphology and Upper Airway Dimensions in Patients with Hypermobile Ehlers-Danlos Syndrome Compared to Healthy Controls

eJournal of Oral Maxillofacial Research, 2021
Objectives: The aims of the present case-control study were to compare craniofacial morphology, airway minimum cross-sectional area and airway volume between patients with hypermobile Ehlers-Danlos syndrome and healthy controls.
Liselotte Sonnesen, Tessie Pawlik, Eva Fejerskov Lauridsen   +2 more
doaj   +1 more source

A case of urinary calculus in a patient with Ehlers‐Danlos syndrome

IJU Case Reports, 2023
Introduction Treatment of urinary tract calculi in patients with Ehlers‐Danlos syndrome, a connective tissue disorder, has rarely been reported. Case presentation A 33‐year‐old woman with Ehlers‐Danlos syndrome sought evaluation of right‐sided abdominal ...
Shunsuke Owa, Yuna Hattori, Shigenori Yonemura, Masaki Sakurai   +3 more
doaj   +1 more source

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

BMC 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, Paulina Adamska, Łukasz Adamski, Aleksandra Sejda, Piotr Wychowański, Michał Studniarek, Barbara Alicja Jereczek-Fossa   +6 more
doaj   +1 more source

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

JA 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, Satoshi Tanaka, Keiko Tsuchiyama, Katsumi Yamamoto, Yuki Maruyama, Kaori Numata, Mikito Kawamata   +6 more
doaj   +1 more source

Investigation into the Ehlers-Danlos syndrome [PDF]

, 1954
Since the 17th century there has been a certain confusion in diagnosis of what is now called the Ehlers-Danlos syndrome. In 1682 Meekrin described the case of a Spaniard who could make his skin stretch to an enormous extent, and appears to have confused ...
Mories, Alexander
core   +3 more sources

Ruptured ulnar artery aneurysm in vascular Ehlers-Danlos syndrome

Journal 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

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

Orphanet 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, Dorothy Luong, Estée C. H. Feldman, Susan Tran, Laure Perrier, Kathleen Eubanks, Mark Bayley, Monika Kastner, Maxwell Slepian, Sarah E. P. Munce   +9 more
doaj   +1 more source

Operative repair of right intrathoracic subclavian artery aneurysms in patients with genetic arteriopathy

Journal of Vascular Surgery Cases and Innovative Techniques, 2023
True intrathoracic subclavian artery aneurysms (SCAAs) are rare and have various etiologies. Right intrathoracic SCAAs pose specific anatomic challenges to repair.
Bryce L. French, MD, Anthony M. Menghini, MS, Christopher R. Burke, MD, Peter H. Byers, MD, Sherene Shalhub, MD, MPH, FACS DFSVS   +4 more
doaj   +1 more source

Ehlers-Danlos syndrome

BMJ Case Reports, 2009
We present a clinical case of a 63-year old Caucasian man with Ehlers-Danlos syndrome who was admitted with atrial fibrillation and arterial hypertension. We present this not as a cardiological case but instead address the key questions of differential diagnosis, diagnosis criteria, management and improving the patient’s quality of life.
Rajin, Choudhury, Valeriu, Revenco, Radu, Darciuc   +2 more
openaire   +3 more sources

Repeated intestinal perforations in vascular Ehlers-Danlos syndrome: a case report of a novel mutation in the COL3A1 gene

Surgical Case Reports, 2023
Background Ehlers-Danlos syndrome is an inherited connective-tissue disorder characterized by skin hyperextensibility, joint hypermobility, and tissue fragility.
Taichi Horino, Yuji Miyamoto, Mayuko Ohuchi, Katsuhiro Ogawa, Naoya Yoshida, Takatoshi Ishiko, Chieko Kukinaka, Rumi Sasaki, Takashi Ohba, Hideo Baba   +9 more
doaj   +1 more source