Results 91 to 100 of about 1,172,427 (185)

Multiple External Invasive Root Resorption and Calcification in Systemic Sclerosis—Case Report

International Endodontic Journal, Volume 59, Issue 9, Page 1963-1978, September 2026.
ABSTRACT Aim There are few reports in the literature of multiple external invasive root resorption (EIRR) lesions in patients with systemic sclerosis (SSc), and an association between root resorption and SSc is not well established. We report the only case that comprehensively illustrates—with the combination of histopathology, cone beam computed ...
Jee‐Yun Leung, Geoffrey Heithersay, Richard Logan, Sharon Liberali   +3 more
wiley   +1 more source

Long‐term outcomes in patients with postural orthostatic tachycardia syndrome with an average follow‐up of over 20 years

Journal of Internal Medicine, Volume 300, Issue 3, Page 299-311, September 2026.
Abstract Background Postural orthostatic tachycardia syndrome (POTS) is a chronic form of orthostatic intolerance that primarily affects female patients. There are scarce data evaluating the long‐term outcomes in POTS. Objectives This study sought to evaluate the long‐term impacts of POTS over multiple decades in adult patients.
Kate M. Bourne, Alfredo Gamboa, Bonnie Black, Juliette Hall, Italo Biaggioni, Cyndya A. Shibao, André Diedrich, Amanda Peltier, Giris Jacob, Luis Okamoto, Robert S. Sheldon, Satish R. Raj   +11 more
wiley   +1 more source

Absence of the inferior labial and lingual frenula in Ehlers-Danlos syndrome

, 2001
The diagnosis of Ehlers-Danlos syndrome Is based on distinctive phenotypical characteristics such as hyperelastic skin and hypermobile joints. To date, no congenital physical markers exist for Identifying patients with Ehlers-Danlos syndrome.
DI MAGGIO, G., Franco Bagnoli, PARRINI, S., Giovanni Di Maggio, Paolo Toti, Claudio De Felice, BAGNOLI, F., Stefano Parrini, TOTI, P., DE FELICE, C.   +9 more
core   +1 more source

Vascular-type Ehlers-Danlos syndrome caused by a hitherto unknown genetic mutation: a case report

Journal of Medical Case Reports, 2013
Introduction Vascular-type Ehlers-Danlos syndrome is an autosomal dominant disease that causes arterial spurting, intestinal perforation, uterine rupture and hemopneumothorax due to decreased production of type III collagen.
Kashizaki Fumihiro, Hatamochi Atsushi, Kamiya Kazunori, Yoshizu Akira, Okamoto Hiroaki   +4 more
doaj   +1 more source

Ehlers–Danlos Syndrome: Not Just Joint Hypermobility

, 2018
Ehlers–Danlos syndrome is an umbrella term for a group of heritable soft connective tissue disorders which is characterized by joint hypermobility, skin texture and elasticity abnormalities, and visceral and vascular fragility or dysfunctions.
Tina Bregant, Milica Klopcic Spevak
core   +1 more source

A case of coexistence of Marfan and Ehlers-Danlos syndromes in a 15-year-old boy

, 2014
Marfan syndrome (MS) and Ehlers-Danlos syndrome (EDS) are examples of two rare genetic diseases characterized by disturbances in the structure of collagen.
Agnieszka Gazda, Zbigniew Swacha, Lidia Rutkowska-Sak   +2 more
core   +1 more source

Retrospective descriptive study of prevalence of symptoms of suspected connective tissue disease: focus on Ehlers-Danlos syndrome

openLo studio analizzerà la prevalenza di sintomi nella Sindrome di Ehlers Danlos cercando di descrivere eventuali sintomi maggiormente significativi per la ...
CALLEGARI, DAVIDE
core  

Ehlers-Danlos syndrome type IV

, 2007
Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous ...
Germain Dominique P
core   +1 more source

Interdisciplinary pain rehabilitation for patients with Ehlers-Danlos syndrome and hypermobility spectrum disorders

Journal of Rehabilitation Medicine
Objective: Chronic pain is a common manifestation of Ehlers-Danlos syndrome and hypermobility spectrum disorders; thus it is often suggested that patients undergo generic interdisciplinary pain rehabilitation, despite there being little evidence to ...
Peter Molander, Mehmed Novo, Åsa Ringqvist, Andrea Hållstam, Hugo Hesser, Monika Löfgren, Britt-Marie Stålnacke, Björn Gerdle   +7 more
doaj   +1 more source

Stroke in Ehlers-Danlos Syndrome Kyphoscoliotic Type: Dissection or Vasculitis?

, 2017
BACKGROUND: Patients with the kyphoscoliotic type of Ehlers-Danlos syndrome have an increased risk of vascular complications such as aortic dissection and perforation. Cerebral ischemia has only rarely been documented.
Martin Wiesmann, Martin Häusler, Kurth, Ingo, Häusler, Martin, Jalaie, Houman, Rohrbach, Marianne, Marianne Rohrbach, Houman Jalaie, Joachim Weis, Ingo Kurth, Weis, Joachim, Häusler, Martin Georg, Wiesmann, Martin, Quade, Annegret, Annegret Quade   +14 more
core   +1 more source