Results 11 to 20 of about 24,908 (251)
Severe conjunctivochalasis in association with classic type Ehlers-Danlos syndrome [PDF]
BMC Ophthalmology, 2012 Background Inferior conjunctivochalasis is common, but is rarely severe enough to require conjunctival excision. This report describes a patient with severe conjunctivochalasis who was subsequently diagnosed with Ehlers Danlos Syndrome, Classic Type ...
Whitaker John K +3 more
doaj +5 more sources
The association between muscle strength and activity limitations in patients with the hypermobility type of Ehlers–Danlos syndrome : the impact of proprioception [PDF]
, 2016 Purpose: The patients diagnosed with Ehlers-Danlos Syndrome Hypermobility Type (EDS-HT) are characterized by pain, proprioceptive inacuity, muscle weakness, potentially leading to activity limitations.
Calders, Patrick +8 more
core +7 more sources
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
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 +3 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