Results 71 to 80 of about 1,279,374 (224)
Ehlers-Danlos syndrome in pregnancy
Journal of Obstetrics and Gynaecology, 2007 A 17-year-old girl with a known diagnosis of vascular type (IV) Ehlers-Danlos syndrome was seen in the antenatal clinic at 9 weeks' gestation.
S, Jaleel, K, Olah
openaire +2 more sources
Haemophilia, EarlyView.ABSTRACT Rare bleeding disorders (RBDs) represent a diverse group of inherited conditions involving coagulation factors or platelets. These conditions, such as Glanzmann thrombasthenia (GT) or severe coagulation factor deficiencies, are uncommon. In contrast, bleeding disorder of unknown cause (BDUC) is a diagnosis of exclusion without an identifiable ...
Alessandro Casini +4 more
wiley +1 more source
GIQLI score (individual spot and means) according to the presence of Ehlers-Danlos syndrome.
, 2013 GIQLI score (individual spot and means) according to the presence of Ehlers-Danlos syndrome.
Benoît Coffin (488926) +6 more
core +1 more source
JPRAS Open, 2019 Combining sutures with adhesive strips to avoid the ‘cheese-wiring’ effect in individuals with fragile skin is a method that has been described previously. Here we demonstrate its application in an individual with Ehlers-Danlos Syndrome. Keywords: Cheese-
S. Shaharan +3 more
doaj +1 more source
Rupture of abdominal aortic aneurysm after spine surgery in the patient with Ehlers-Danlos syndrome -A case report- [PDF]
Korean Journal of Anesthesiology, 2010 Ehlers-Danlos syndrome (EDS) is a rare inherited disorder of the connective tissue that is characterized by hyperextensible skin, hypermobile joints and abnormalities of the cardiovascular system.
Jung Sik Im +4 more
doaj +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
International Journal of Gynecology &Obstetrics, Volume 169, Issue 1, Page 421-423, April 2025.
Peter H. Cygan +3 more
wiley +1 more source
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
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 +2 more
core +1 more source
Az Ehlers–Danlos-szindrómák korszerű osztályozása és multidiszciplináris tünettana = Up-to-date classification and multidisciplinary symptoms of Ehlers–Danlos syndromes [PDF]
, 2019 Absztrakt: A szerzők a ritka, örökletes kötőszöveti betegségek közé tartozó Ehlers–Danlos-szindrómacsoportra vonatkozó korszerű, nemzetközi osztályozáson alapuló klinikai ismereteket foglalják ...
Márta Medvecz +9 more
core +1 more source