Results 11 to 20 of about 24,909 (251)
Gender dysphoria in adolescents with Ehlers–Danlos syndrome
SAGE Open Medicine, 2022 Objectives: Ehlers–Danlos Syndrome represents a family of heritable connective tissue disorders that include joint hypermobility, tissue fragility, and skin hyperextensibility.
Jordan T. Jones +4 more
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Pediatric Innominate Artery Pseudoaneurysm Rupture in Vascular Ehlers-Danlos Syndrome: A Case Report
Clinical Practice and Cases in Emergency Medicine, 2021 Introduction: Ehlers-Danlos syndrome is a well classified connective tissue disorder recognized by its features of hyperextensibility of joints and hyperelasticity of the skin.
Aimee Vos, Katharine M. Burns
doaj +1 more source
Indian Dermatology Online Journal, 2014 Ehlers-Danlos syndrome (EDS) is a generalized disorder of one element of connective tissue manifesting clinically by fragility and hyperelasticity of the skin and joint laxity. It is a hereditary disorder, the inheritance being usually autosomal dominant with low penetrance. Autosomal recessive and X-linked recessive varieties are also known.
Farhana Tahseen Taj +2 more
openaire +5 more sources
Warmblood fragile foal syndrome type 1 mutation (PLOD1 c.2032G>A) is not associated with catastrophic breakdown and has a low allele frequency in the Thoroughbred breed. [PDF]
, 2020 BackgroundCatastrophic fractures are among the most common cause of fatalities in racehorses. Several factors, including genetics, likely contribute to increased risk for fatal injuries.
Arthur, R +6 more
core +1 more source
South African Medical Journal, 2016 The Ehlers-Danlos syndromes (EDSs) were originally described by Ehlers in Denmark and Danlos in Paris in 1898 and 1908, respectively. They had both published individual case studies in which the common factor was laxity of ligaments leading to joint hypermobility and hyperextensibility of the skin.
Leganger, Julie +5 more
openaire +6 more sources
BMJ, 2007 These three case histories illustrate the many problems facing patients with Ehlers-Danlos syndrome in its various ...
Frances, Gawthrop +3 more
openaire +2 more sources
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 +2 more
openaire +4 more sources
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 +2 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 +6 more
doaj +1 more source
Superior Semicircular Canal Dehiscence in a Patient with Ehlers-Danlos Syndrome: A Case Report. [PDF]
, 2017 Superior semicircular canal dehiscence (SSCD) is a bony defect in the middle cranial fossa floor that results in an abnormal connection between the inner ear and cranial vault.
Chung, Lawrance K +4 more
core +1 more source