Zobrazeno 1 - 10
of 796
pro vyhledávání: '"rendu osler"'
Autor:
Ouiam Elmqaddem, Hajar Koulali, Abdelkrim Zazour, Meryem Nasiri, Moulay Zahi Ismaili, Ghizlane Kharrasse
Publikováno v:
Radiology Case Reports, Vol 19, Iss 9, Pp 3810-3813 (2024)
Osler-Weber-Rendu disease (OWRD), also known as hereditary haemorrhagic telangiectasia (HHT), is an autosomal dominant genetic disorder characterised by arteriovenous malformations in several organs. Ischemic cholangitis is a rare life-threatening co
Externí odkaz:
https://doaj.org/article/b74563ccfc34487999b2891c32b49ffe
Publikováno v:
CVIR Endovascular, Vol 7, Iss 1, Pp 1-4 (2024)
Abstract Background Renal arteriovenous malformation (AVM) in Hereditary Hemorrhagic Telangiectasia (HHT) is uncommon and only few cases have been described, mainly with surgical management because of uncontrolled hematuria. Case presentation We mana
Externí odkaz:
https://doaj.org/article/e58073af6f744341b51a641a16696dce
Autor:
Marcel Stodolak, Aleksandra Krużel, Kamil Kłos, Piotr Sajdak, Justyna Tomasik, Marika Dębik, Łukasz Szydłowski, Klaudia Żurowska, Seweryn Ziajor, Artur Bednarski, Mikołaj Turski
Publikováno v:
Journal of Education, Health and Sport, Vol 65 (2024)
Introduction and purpose: Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is a rare and complex vascular disorder characterized by abnormal blood vessel formation. It can present significant challenges in diagno
Externí odkaz:
https://doaj.org/article/34c5932bdb26489e807103c5e6ecf910
Autor:
Cristiane Ferreira de Araújo-Gomes, Carlos Eduardo Virgini-Magalhães, Leonardo Silveira de Castro, Eduardo de Oliveira Rodrigues Neto, Alex Antunes Bezerra, Monica Rochedo Mayall, Cristina Ribeiro Riguetti-Pinto, Felipe Borges Fagundes
Publikováno v:
Jornal Vascular Brasileiro, Vol 23 (2024)
Resumo A síndrome de Rendu-Osler-Weber, também conhecida como telangiectasia hemorrágica hereditária, é uma doença hereditária autossômica dominante. Ela é caracterizada pela presença de múltiplas malformações arteriovenosas e telangiect
Externí odkaz:
https://doaj.org/article/c45058d9f96f4fc8a41d38f8140f9d47
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 15, Iss 6, Pp 78-84 (2023)
Clarification of the aetiology of ischemic stroke (IS) in young adults (aged between 18 and 45 years) is an extremely difficult task, as rare causes that are hardly known to neurologists are very common. One of these causes is paradoxical embolism du
Externí odkaz:
https://doaj.org/article/ffd2a65a126c4330a23e78be9423d7a1
Autor:
Maria A. Mozdon, Rodion V. Ponomarev, Nina V. Tsvetaeva, Aleksey V. Shabrin, Evgeniya I. Ermachenkova, Sergei E. Larichev, Elena A. Lukina
Publikováno v:
Терапевтический архив, Vol 95, Iss 7, Pp 580-585 (2023)
RenduOslerWeber disease or hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease. It is characterized by vascular dysplasia with the formation of telangiectasias on the skin, mucous membranes of the respiratory and digestiv
Externí odkaz:
https://doaj.org/article/27090d2f6f9a436b86f0f02c1fa3aced
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 19, Iss 2, Pp 179-185 (2023)
A 64-year-old female with a family history of hereditary hemorrhagic telangiectasia (HHT) was hospitalized due to complaints of dyspnea during light physical exertion and leg edema. HHT was diagnosed at 20 y.o., recurrent nasal bleeding started at ag
Externí odkaz:
https://doaj.org/article/0d4b23c48c334811a007ab23a435eedd
Publikováno v:
BMC Ophthalmology, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Background Hereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome is a bleeding disorder that can affect all parts of the body including the eyes. Different ocular abnormalities have been described in relation
Externí odkaz:
https://doaj.org/article/e9834b15f071400c8a9f5c3948b6756f
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