Results 81 to 90 of about 5,408,282 (157)
Biomolecules & Biomedicine, 2017 Hepatopulmonary syndrome (HPS) is a severe complication of advanced liver disease associated with an extremely poor prognosis. HPS is diagnosed in 4-47% of patients with cirrhosis and in 15-20% of candidates for liver transplantation.
Inna Krynytska +6 more
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Rendu-Osler-Weber Syndrome: A Case Report [PDF]
, 2014 Hereditary hemorrhagic telangectasia (HHT) or Rendu-Osler-Weber syndrome, is a rare genetic disorder with autosomal dominance and variable penetrance. The typical findings of the disease are telangiectasias in skin and mucous membranes, and arteriovenous
Ignjatović, Vesna +3 more
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Rendu-Osler-Weber syndrome and ocular manifestations in hereditary hemorrhagic telangiectasia [PDF]
, 1992 The relatively rare syndrome of Rendu-Osler-Weber and the associated hemorrhagic telangiectasia present with various ocular signs, such as telangiectases of the lids, conjunctiva, and retina.
Jenisch, Daniel A
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Osler-Weber-Rendu syndrome - Pathological manifestations and autopsy considerations
, 2001 An 18-year-old university student with Osler-Weber-Rendu disease collapsed in the bathroom. Attempted resuscitation was unsuccessful. Her past history included recurrent epistaxes, mucosal telangiectasias, intracranial arteriovenous malformations with ...
Byard, R., Schliebs, J., Koszyca, B.
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Fibrodysplastic implications for transvenous embolization of a high-flow pelvic arteriovenous malformation in Osler-Weber-Rendu syndrome [PDF]
, 2015 Osler-Weber-Rendu syndrome is a rare genetic disorder that commonly features high-flow arteriovenous malformations (AVM) within the pulmonary, intracranial, and visceral circulation.
Nassiri, Naiem +2 more
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Respiratory Medicine Case Reports, 2018 We present a case series of four siblings with hereditary hemorrhagic telangiectasia (HHT) and pulmonary arteriovenous malformations (PAVM). The patients' mother has HHT. Case 1: A 22-year-old man developed dyspnea and epistaxis. CT revealed a large PAVM,
Keiki Yokoo +11 more
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Angiomatosis in Klippel-Trenaunay -Weber Syndrome - Report of a rare Case
Journal of Indian Academy of Oral Medicine and Radiology, 2006 Hemangioma is an abnormal proliferation of blood vessels that may occur in any vascularized tissue. Considerable debate exists as to whether these lesions are neoplasms, hamartomas, or vascular malformations.
G S Kodhandarama +2 more
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UEG Week 2025 Poster Presentations
United European Gastroenterology Journal, Volume 13, Issue S8, Page S803-S1476, October 2025.
wiley +1 more source
Revista Cubana de Hematología, Inmunología y Hemoterapia, 2012 Los pacientes con epístaxis representan entre el 10 y 12 % de los casos atendidos en los servicios de urgencia de otorrinolaringología. Se presentan 5 pacientes atendidos en este servicio del Hospital General Docente "Enrique Cabrera", en el período ...
Tahamara Alcalá-Villalón +2 more
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International Journal of Vascular Medicine, 2019 Pulmonary arterial hypertension (PAH) can be discovered in patients who have a loss of function mutation of activin A receptor-like type 1 (ACVRL1) gene, a bone morphogenetic protein (BMP) type 1 receptor.
Vincent Avecilla
doaj +1 more source