Results 91 to 100 of about 6,765 (189)

Familial cerebral abscesses caused by hereditary hemorrhagic telangiectasia [PDF]

, 2017
In case of a cerebral abscess without known cause, Pulmonary arteriovenous malformations (PAVM) screening should be performed. If PAVM(s) is identified, Hereditary hemorrhagic telangiectasia (HHT) is very likely and should always be considered. This case
I Dali, Christine, Lauridsen, Mathilde Faurholdt, Lillian Bomme Ousager, Pernille Mathiesen Tørring, Andersen, Poul Erik, Mathilde Faurholdt Lauridsen, Poul Erik Andersen, Brusgaard, Klaus, Tørring, Pernille Mathiesen, Anette Kjeldsen, Ousager, Lilian Bomme; id_orcid, Kjeldsen, Anette Drøhse; id_orcid, Klaus Brusgaard, Christine i Dali   +13 more
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Malformações arteriovenosas pulmonares: Associação a telangiectasia hemorrágica hereditária Casos clínicos e rastreio familiar Pulmonary arteriovenous malformations: Association with hereditary hemorrhagic telangiectasia. Clinical cases and family screening

Revista Portuguesa de Pneumologia, 2006
As malformações arteriovenosas pulmonares são raras e mais de metade dos casos surgem em associação a telangiectasia hemorrágica hereditária. Faz-se uma revisão teórica sobre a apresentação clínica, abordagem diagnóstica, terapêutica e prognóstico destas
Diva Ferreira, Joana Amado, Raquel Duarte, José Almeida, Paulo Morgado, Teresa Shiang   +5 more
doaj  

Telangiectasia hemorrágica hereditaria Hereditary hemorrhagic telangiectasia

Medisan, 2009
Se presenta el caso de una paciente de 52 años de edad, con antecedentes de hipertensión arterial desde hace cinco años, que acudió a consulta por presentar sangrado a nivel de la lengua en reiteradas ocasiones, desencadenados por pequeños traumatismos ...
Raymundo Rafael Fernández Díaz, Tania Ricardo Falcón, Roxana Collado Yero   +2 more
doaj  

Familial manifestation of hereditary hemorrhagic telangiectasia

, 2016
Segundo a Organização Mundial de Saúde, as doenças são consideradas raras quando afetam até 65 pessoas em cada 100.000 indivíduos, ou seja, 1,3 para cada 2.000 pessoas.
Natália Martins Joaquim
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Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia

, 2001
BACKGROUND: Most patients with familial primary pulmonary hypertension have defects in the gene for bone morphogenetic protein receptor II (BMPR2), a member of the transforming growth factor beta (TGF-beta) superfamily of receptors. Because patients with
N. Galie (7688801), M. Pauciulo (17188999), C. Atkinson (7688795), J. McGaughran (17253364), N. V. Morgan (17253370), R. C. Trembath (7628618), J. Berg (6109451), J. R. Thomson (2905727), N. W. Morrell (7688810), J. E. Loyd (7688804), I. Winship (7621277), A. Manes (17253361), M. Humbert (762823), L. Wheeler (17253367), W .C. Nichols (17253373), Rajiv Machado (17162539), G. Simonneau (7688798)   +16 more
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Future treatments for hereditary hemorrhagic telangiectasia

Orphanet Journal of Rare Diseases, 2020
Hereditary Hemorrhagic Telangiectasia (HHT), also known as Rendu-Osler syndrome, is a genetic vascular disorder affecting 1 in 5000–8000 individuals worldwide.
Florian Robert, Agnès Desroches-Castan, Sabine Bailly, Sophie Dupuis-Girod, Jean-Jacques Feige   +4 more
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Hereditary Hemorrhagic Telangiectasia in a Sudanese Patient

, 2020
Background. Hereditary hemorrhagic telangiectasia (HHT) also known as Osler–Weber–Rendu syndrome is a rare autosomal dominant disorder, which results in vascular dysplasia affecting mainly visceral and mucocutaneous organs. Case Presentation.
Ahmed Abdalazim Dafallah Albashir, Omer Ali Mohamed Ahmed Elawad, Ahmed Ali Mohamed Ahmed Elawad, Mohammed Mahgoub Mirghani Ahmed, Osman Eltieb Elbasheer Mohamed   +4 more
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Benefits of Treating Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Retrospective Analysis of 14 Patients

World Neurosurgery: X, 2019
Background: Arteriovenous malformations (AVMs) are a cardinal feature of hereditary hemorrhagic telangiectasia (HHT). However, whether to treat brain AVMs in patients with HHT remains questionable because of the possible risks.
M. Neil Woodall, Peter Nakaji, Robert F. Spetzler   +2 more
doaj   +1 more source

Efficacy of low-dose Bevacizumab in Hereditary Hemorrhagic Telangiectasia

, 2011
not ...
Lastella P., Suppressa P, Valerio R., Sabbà C., Punzi G., Lenato GM   +5 more
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Ocular manifestations in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): A case-series.

, 2011
BACKGROUND: Hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease) is an autosomal dominant vascular disorder characterized by severe and recurrent nosebleeds, muco-cutaneous telangiectasias, and, in some cases, life-threatening visceral ...
Porcellini A, Chiosi F., De Benedictis A., Rinaldi M., Costagliola C., RINALDI, Michele, Danesino C., Buscarini E, Danesino C, Chiosi F, Buscarini E., PORCELLINI, ANTONIO, De Benedictis A   +12 more
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