Ehlers-danlos syndrome - Open Access .click

Results 71 to 80 of about 1,170,712 (223)

Proceedings of the Royal Society of Medicine, 1939
F P, Weber, H, Huber
+9 more sources

Menstrual suppression to decrease intrauterine device expulsion in adolescents with inherited bleeding disorders

International Journal of Gynecology &Obstetrics, Volume 169, Issue 1, Page 421-423, April 2025.
Peter H. Cygan +3 more
wiley +1 more source

Underlying Ehlers-Danlos syndrome discovered during neuro-ophthalmic evaluation of concussion patients: a case series

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

Successful coil embolization for rupture of the subclavian artery associated with Ehlers-Danlos syndrome type IV [PDF]

, 2009
Ehlers-Danlos syndrome is a rare inherited disease of connective tissue. Patients with type IV Ehlers-Danlos syndrome are likely to present with arterial disorders such as aneurysm or dissection.
Obitsu, Yukio +3 more
core +1 more source

Cardiovascular, autonomic symptoms and quality of life in children with hypermobile Ehlers–Danlos syndrome

SAGE Open Medicine
Objectives: 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

[A case of Ehlers-Danlos syndrome].

Shoni shikagaku zasshi. The Japanese journal of pedodontics, 1989
Ehlers-Danlos syndrome, an inherited connective tissue disorder, is characterized by skin hyperextensibility, joint hypermobility and skin fragility. The disease is at least classified into 10 types, I to X, based on clinical features, biochemical abnormalities of the connective tissue and the mode of inheritance.
Seki, Mitsuko +3 more
openaire +2 more sources

Genetic risk variants implicate impaired maintenance and repair of periodontal tissues as causal for periodontitis—A synthesis of recent findings

Periodontology 2000, EarlyView.
AbstractPeriodontitis is a complex inflammatory disease in which the host genome, in conjunction with extrinsic factors, determines susceptibility and progression. Genetic predisposition is the strongest risk factor in the first decades of life. As people age, chronic exposure to the periodontal microbiome puts a strain on the proper maintenance of ...
Arne S. Schaefer +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

Multiple dermatofibromas in a patient with Ehlers–Danlos syndrome: a case report

Journal of Medical Case Reports
Background 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

humans
3. good health
female

adult
joint instability
ehlers–danlos syndrome

male
pregnancy
adolescent