Results 71 to 80 of about 1,012,341 (230)
Oral Manifestations of Non Vascular Ehlers‐Danlos Syndrome Cross‐Sectional Study
Oral Diseases, EarlyView.ABSTRACT Background Ehlers–Danlos syndromes are rare hereditary connective tissue disorders; however, their oral manifestations remain poorly characterized in molecularly confirmed individuals. The aim of this study was to describe the oral phenotype of patients with non‐vascular Ehlers‐Danlos syndromes compared to healthy controls.
Aude Grand +4 more
wiley +1 more source
Ehlers-Danlos syndrome associated with acute pancreatitis [PDF]
, 1989 The Ehlers-Danlos syndrome is a polysystemic inherited connective tissue disease characterized by articular laxity, hyperelastic skin, a tendency to excessive bleeding in the presence of minimal trauma, and friability of different tissues.
Jimenez,, Sarra-Carbonell,
core
BMC Ophthalmology, 2019 Background The Ehlers-Danlos syndromes are a heterogenous group of diseases that cause connective tissue defects. At present, there are no published reports focusing upon the neuro-ophthalmic symptoms that might occur in EDS patients after mild traumatic
Abhishek Gami, Eric L. Singman
doaj +1 more source
International Journal of Gynecology &Obstetrics, Volume 169, Issue 1, Page 421-423, April 2025.
Peter H. Cygan +3 more
wiley +1 more source
Solitary Lesion With Features of Atrophic Papulosis in Early Childhood
Pediatric Dermatology, EarlyView.ABSTRACT Atrophic papulosis (Köhlmeier‐Degos disease) is a rare thrombo‐occlusive vasculopathy classically presenting with multiple porcelain‐white atrophic papules and a high risk of progression to systemic involvement. We report a 2‐year‐old girl presenting with clinical, dermoscopic, and histologic findings of atrophic papulosis with only a solitary
Ou Jia Emilie Wang +4 more
wiley +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
SAGE Open MedicineObjectives: Hypermobile Ehlers–Danlos syndrome is a connective tissue disorder characterized by joint hypermobility and other systemic manifestations. Cardiovascular, autonomic symptoms and dysautonomia are frequently reported in adults with hypermobile ...
Amanda K Hertel +5 more
doaj +1 more source
Unilateral periventricular heterotopia and epilepsy in a girl with Ehlers–Danlos syndrome
Epilepsy and Behavior Case Reports, 2015 Purpose: Ehlers–Danlos syndrome (EDS), comprising a variety of inherited connective tissue disorders, has already been described in association with various neurological features, particularly with epilepsy and periventricular heterotopia (PH). Until now,
Salvatore Savasta +5 more
doaj +1 more source
Multiple dermatofibromas in a patient with Ehlers–Danlos syndrome: a case report
Journal of Medical Case ReportsBackground Dermatofibromas, also known as benign fibrous histiocytomas, are among the most common cutaneous soft-tissue lesions. Association of multiple dermatofibromas with some diseases was described and it has not been reported with Ehlers–Danlos ...
Fatemeh Mohaghegh +3 more
doaj +1 more source