Results 61 to 70 of about 20,981 (109)
, 2019 Introduction: Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant genetic disease characterized by the presence of arteriovenous malformations in the nasal mucosa, the tips of fingers, and sometimes in the lungs, the gastrointestinal ...
Prada-Arismendy, Jeanette +1 more
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Telangiectasia hemorrágica hereditaria: utilidad de los anticuerpos monoclonales en su tratamiento
, 2011 The Hereditary Hemorrhagic Telangiectasia is a progressive multisystem vascular dysplasia characterized by mucocutaneous telangiectasias and arteriovenous connections. Its most common symptomatology is recurrent epistaxis, with iron deficiency anemia, so
Mendieta Eckert, Marta +3 more
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Closure of the nasal cavities in the treatment of refractory hereditary haemorrhagic telangiectasia [PDF]
, 1997 From a cohort of 35 patients with hereditary haemorrhagic telangiectasia (HHT), 12 patients have undergone closure of the one or both nasal cavities during the last three years for refractory epistaxis.
Howard, DJ, Lund, VJ
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Enfermedad de Osler-Weber-Rendu o telangiectasia hemorrágica hereditaria. Informe de caso [PDF]
Introduction: hereditary hemorrhagic telangiectasia or Osler-Weber-Rendu disease is of genetic origin and is rare. Patients present anomalous communications between arterioles and venules, and specific malformations in internal organs.
Pages Morales, Nidhessy +2 more
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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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Telangiectasia hemorrágica hereditaria Enfermedad de Osler Weber Rendu
, 2016 Resumen: La telangiectasia hemorrágica hereditaria (THH) o el síndrome de Osler Weber Rendu, es una enfermedad autosómica dominante caracterizada por telangectasias mucocutaneas, epistaxis y sangrados digestivos recurrentes y por el desarrollo de ...
Vargas Castro,María Paula
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The Pan-American Journal of Ophthalmology, 2017 Haemolacria is a rare term that expresses the presence of blood cells in tears. It is commonly a benign process with diverse etiologies, from vascular diseases, trauma and neoplasms.
Claudio Martin Franco de Acha +1 more
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43° Congreso Nacional de la Sociedad Española de Medicina Interna (SEMI): Gijón, 23-25 de Noviembre de 2022. [PDF]
Rev Clin Esp, 2023 europepmc +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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