Results 21 to 30 of about 11,240 (218)
Circulatory contributors to the phenotype in hereditary hemorrhagic telangiectasia [PDF]
, 2015 Hereditary hemorrhagic telangiectasia (HHT) is mechanistically and therapeutically challenging, not only because of the molecular and cellular perturbations that generate vascular abnormalities, but also the modifications to circulatory physiology that ...
Shovlin, CL
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Pulmonary arteriovenous malformation
Journal of the Belgian Society of Radiology, 2011 A 37-year old patient with Rendu-Osler-Weber syndrome presented to our hospital with hypoxy.
Janssens, E +4 more
openaire +7 more sources
Hemangioma – A pointer to Abernethy syndrome?
Annals of Pediatric Cardiology, 2020 Diffuse pulmonary arteriovenous malformations or pulmonary arterial hypertension (PAH) may result from congenital portosystemic venous shunts. Hemangioma as a physical sign of congenital portosystemic shunts (like Abernethy syndrome) has not been ...
Shyam S Kothari
doaj +1 more source
Severe hepatic and pulmonary involvement in Rendu-Osler-Weber syndrome [PDF]
, 2018 We report the case of a young woman with hereditary hemorrhagic telangiectasia (HHT) with severe liver involvement and pulmonary shunting. The medical imaging in this patient illustrates the severe shunting that can occur in these patients who often are ...
Geerts, Anja +4 more
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Management of Pulmonary Arteriovenous Malformations [PDF]
Seminars in Interventional Radiology, 2011 Pulmonary arteriovenous malformations are rare lesions with significant clinical complications. These lesions are commonly seen in patients with hereditary hemorrhagic telangiectasia (formerly Osler-Weber-Rendu syndrome). Interventional radiologists are a key part of the treatment team in this complex disease, and a thorough understanding of the ...
Mary E, Meek +2 more
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Giant pulmonary arteriovenous malformation [PDF]
European Journal of Cardio-Thoracic Surgery, 2004 A 44-year-old man was admitted with coughing and dyspnea for 3 weeks. Chest radiography and thoracic CT scanning confirmed a huge left lung arteriovenous malformation (Fig. 1). Due to a prohibitively high operative risk, he was investigated with pulmonary angiography in preparation for embolization therapy (Fig. 2). The patient subsequently refused all
Sihoe, ADL +3 more
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Journal of Pediatric Surgery Case Reports, 2015 Patients with hepatic arteriovenous malformations rarely present with pulmonary hypertension. We report the case of a 3-month-old boy who developed severe pulmonary hypertension due to a hepatic arteriovenous malformation.
Naruhiko Murase +8 more
doaj +1 more source
Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia. [PDF]
, 2003 BACKGROUND\ud \ud Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).
Abdalla, S A +16 more
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JA Clinical Reports, 2023 Background Osler-Weber-Rendu syndrome is characterized by mucocutaneous telangiectasia and arteriovenous malformations in organs. Anesthesia for patients with Osler-Weber-Rendu syndrome is challenging due to complications and physiological changes.
Toshiharu Hiyoshi +4 more
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The roles of endoglin gene in cerebrovascular diseases. [PDF]
, 2017 Endoglin (ENG, also known as CD105) is a transforming growth factor β (TGFβ) associated receptor and is required for both vasculogenesis and angiogenesis.
Ma, Li, Su, Hua, Zhang, Rui, Zhu, Wan
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