Results 21 to 30 of about 1,555,246 (206)

Vascular Ehlers-Danlos syndrome with distinct histopathologic features [PDF]

Journal of Pathology and Translational Medicine, 2022
Ehlers-Danlos syndrome is a connective tissue disorders that presents with heterogeneous manifestations depending on the involved genes. Vascular Ehlers-Danlos syndrome (vEDS), also known as Ehlers-Danlos syndrome type IV, is caused by a heterozygous ...
Hee Sang Hwang, Jin Woo Song, Se Jin Jang   +2 more
openaire   +4 more sources

Vascular Ehlers-Danlos Syndrome and Pregnancy: A Systematic Review

Obstetric Anesthesia Digest
(BJOG. 2024;131:1620-1629. doi: 10.1111/1471-0528.17893) The prevalence of Ehlers-Danlos syndrome (EDS) is ∼1 in 5000, and it is characterized by joint hyperlaxity, high skin elasticity, and fragile connective tissue. There are 13 known subtypes, and the most frequently occurring of these are classic EDS, hypermobile EDS, and vascular EDS ...
Haem, Théo, Benson, Betty, Dernoncourt, Amandine, Gondry, Jean, Schmidt, Jean, Foulon, Arthur   +5 more
openaire   +3 more sources

Genetic testing for vascular Ehlers-Danlos syndrome and other variants with fragility of the middle arteries

The EuroBiotech Journal, 2018
Ehlers-Danlos syndrome (EDS) is an umbrella term for various inherited connective tissue disorders associated with mutations in genes involved in extracellular matrix formation.
Rakhmanov Yeltay, Maltese Paolo Enrico, Bruson Alice, Castori Marco, Beccari Tommaso, Dundar Munis, Bertelli Matteo   +6 more
doaj   +2 more sources

Adults with Loeys-Dietz syndrome and vascular Ehlers-Danlos syndrome: A cross-sectional study of life satisfaction

Journal of Rehabilitation Medicine, 2021
Objective: To explore life satisfaction among adults with Loeys-Dietz and those with vascular Ehlers-Danlos syndrome. Design: Postal survey in 2018. Participants and methods: Persons with molecularly verified Loeys-Dietz syndrome or vascular Ehlers ...
Heidi Johansen, Gry Velvin, Kerstin Fugl-Meyer, Ingeborg Beate Lidal   +3 more
doaj   +1 more source

Vascular Ehlers Danlos syndrome [PDF]

Circulation: Cardiovascular Genetics, 2014
Vascular Ehlers–Danlos syndrome (vEDS) is an autosomal dominant disease that affects the arteries, bowels, uterus, and skin. Affected individuals can have spontaneous rupture of hollow organs, such as the bowels or gravid uterus, along with arterial dissections and ruptures that lead to premature death.
Yuranga Weerakkody, Francis Fortin, Bruno Di Muzio   +2 more
openaire   +3 more sources

Prevalence of Scoliosis in Hypermobile Ehlers-Danlos Syndrome [PDF]

, 2021
Objective: The main purpose of this study was to evaluate the prevalence, form, and severity of scoliosis in a population of adults meeting the 2017 criteria for hypermobile Ehlers-Danlos syndrome (hEDS).
Robert Carlier, Malika Foy, Fabrice Gillas, Ahmed Mekki, Karelle Benistan   +4 more
core   +1 more source

Repeated intestinal perforations in vascular Ehlers-Danlos syndrome: a case report of a novel mutation in the COL3A1 gene

Surgical Case Reports, 2023
Background Ehlers-Danlos syndrome is an inherited connective-tissue disorder characterized by skin hyperextensibility, joint hypermobility, and tissue fragility.
Taichi Horino, Yuji Miyamoto, Mayuko Ohuchi, Katsuhiro Ogawa, Naoya Yoshida, Takatoshi Ishiko, Chieko Kukinaka, Rumi Sasaki, Takashi Ohba, Hideo Baba   +9 more
doaj   +1 more source

Vascular Ehlers Danlos syndrome

Journal of Pediatric Gastroenterology and Nutrition, 2018
Clinical History Image Findings Discussion Find Diagnosis Differential ...
Loeys, Bart, De Backer, Julie, Pope, FM
  +6 more sources

Elastosis perforans serpiginosa related to vascular Ehlers-Danlos syndrome [PDF]

, 2019
Elastosis perforans serpiginosa (EPS) is a rare skin disease with elimination of connective tissue fibers from dermis to epidermis. The typical presentation shows hyperkeratotic red or skin-colored papules arranged in a circinate pattern. We present a 26-
Uldall Pallesen, Kristine Appel, Bygum, Anette, Lindahl, Kim Hein   +2 more
core   +5 more sources

Ruptured ulnar artery aneurysm in vascular Ehlers-Danlos syndrome

Journal of Vascular Surgery Cases and Innovative Techniques, 2020
Vascular Ehlers-Danlos syndrome (vEDS), also known as type IV Ehlers-Danlos syndrome, is a rare inherited connective tissue disease that affects 1 in 50,000 to 250,000 individuals.
Ryan Howard, MD, Nicholas Osborne, MD
doaj   +1 more source