Results 41 to 50 of about 1,915,478 (171)

Iliac artery aneurysm endoleak management in a patient with vascular Ehlers-Danlos syndrome

Journal of Vascular Surgery Cases and Innovative Techniques
Endovascular repair has traditionally been avoided in patients with connective tissue disorders. We describe successful treatment of multiple endoleaks of an expanding common iliac artery aneurysm previously treated with an endograft in a patient with ...
Mitri K. Khoury, MD, Matthew J. Eagleton, MD   +1 more
doaj   +1 more source

Colonoscopic perforation leading to a diagnosis of Ehlers Danlos syndrome type IV: a case report and review of the literature

Journal of Medical Case Reports, 2011
Introduction Colonoscopic perforation is a rare but serious complication of colonoscopy. Factors known to increase the risk of perforation include colonic strictures, extensive diverticulosis, and friable tissues.
Wolfe John, Lloyd Josephine, Purkayastha Sanjay, Aziz Omer, Rana Mariam, Ziprin Paul   +5 more
doaj   +1 more source

The association between collagenopathies and the risk of spontaneous preterm birth: A systematic review with selective meta‐analysis

Acta Obstetricia et Gynecologica Scandinavica, EarlyView.
This review quantifies the association between collagenopathies and spontaneous preterm birth, assessing their role in antenatal risk assessment. Marfan syndrome is significantly associated with an increased risk of spontaneous preterm birth (OR 2.71, 95% CI 2.23–3.30; p < 0.001; I2 = 41%) while evidence for Ehlers–Danlos syndrome is heterogeneous ...
Kensie Treacy, Brenda F. Narice, Denya Williams‐Goss, Dilly O. C. Anumba   +3 more
wiley   +1 more source

Síndrome de Ehlers-Danlos e gravidez: relato de caso Ehlers-Danlos syndrome and pregnancy: a case report

Revista Brasileira de Ginecologia e Obstetrícia, 2003
A síndrome de Ehlers-Danlos é doença do tecido conjuntivo cuja associação com a gestação é extremamente rara, mas com complicações potencialmente fatais no ciclo gravídico-puerperal, como roturas vasculares e intestinais.
Marcelo Luís Nomura, Fernanda Garanhani de Castro Surita, Mary Angela Parpinelli   +2 more
doaj   +1 more source

Rare Bleeding Disorders and Bleeding Disorder of Unknown Cause: Current Understanding and Recent Developments

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, Robert Klamroth, Bauke Haisma, Dino Mehic, Saskia E. M. Schols   +4 more
wiley   +1 more source

Multidisciplinary hybrid approach to management of a thoracoabdominal aneurysm in a patient with both Loeys-Dietz and vascular Ehlers-Danlos syndrome

Journal of Vascular Surgery Cases and Innovative Techniques
Loeys-Dietz syndrome and vascular Ehlers-Danlos syndrome are genetic aortopathies that result from abnormal collagen matrix formation associated with vascular complications and early death.
Nicolas A. Stafforini, MD, Nallely Saldana-Ruiz, MD, MPH, Scott DeRoo, MD, Ulrike Schwarze, MD, Matthew P. Sweet, MD, Sara L. Zettervall, MD, MPH   +5 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, Alennie Lopez, Nathan Teegee, Richard I. Crawford, Joseph M. Lam   +4 more
wiley   +1 more source

Ehlers-Danlos with disease of the aorta and mitral valve

, 2012
A woman aged 46 years with a history of vascular Ehlers Danlos syndrome presented with atypical chest pain. She had previously required a mitral valve replacement for mitral valve prolapse.
Pearman, Charles M.
core   +1 more source

Spontaneous celiac artery aneurysms in 13-year-old and 10-year-old brothers with PLOD1-related kyphoscoliotic Ehlers-Danlos syndrome

Journal of Vascular Surgery Cases and Innovative Techniques
PLOD1-related kyphoscoliotic Ehlers-Danlos syndrome is a rare, autosomal recessive connective tissue disorder characterized by congenital hypotonia, early-onset, progressive kyphoscoliosis, and generalized joint hypermobility. PLOD1-kyphoscoliotic Ehlers-
Apoorva Bhandari, MD, MSc, Victoria Siu, MD, FRCPC, FCCMG, Audra A. Duncan, MD, FACS, FRCSC   +2 more
doaj   +1 more source

Gastric perforation leading to the diagnosis of classic Ehlers–Danlos syndrome: a case report

Journal of Medical Case Reports, 2021
Background Ehlers–Danlos syndrome is a clinically and genetically heterogeneous group of heritable connective tissue disorders caused by a defect in collagen synthesis and structure.
Ahad E. Alotaibi, Ohood H. AlAamer, Mohammed A. Bawazeer, Ali A. Alzahrani   +3 more
doaj   +1 more source