Results 41 to 50 of about 5,408,332 (199)

Computed Tomography Imaging Findings of Hepatic Hereditary Haemorrhagic Telangiectasia [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2018
Hereditary Haemorrhagic Telangiectasia (HHT) also known as Osler Weber Rendu disease is a rare, under diagnosed, autosomal dominant multiorgan angio dysplasia.
Nayna Goyal   +4 more
doaj   +1 more source

Rendu-Osler-Weber Disease with High Pulmonary Hypertension and Interstitial Lung Disease

open access: yesРациональная фармакотерапия в кардиологии, 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 age 52,
Yu. A. Lutokhina   +3 more
doaj   +1 more source

Novel mutation in ENG gene causing Hereditary Hemorrhagic Telangiectasia in a Peruvian family [PDF]

open access: yesGenetics and Molecular Biology, 2020
Hereditary Hemorrhagic Telangiectasia (HHT) is a rare disorder of vascular development. Common manifestations include epistaxis, telangiectasias and arteriovenous malformations (AVMs) in multiple organs. Most patients have deletions or missense mutations
Alejandro Zevallos-Morales   +9 more
doaj   +1 more source

Thalidomide as an effective treatment in a case of Osler Weber Rendu syndrome: a case report

open access: yesAsian Journal of Medical Sciences, 2016
Osler Weber Rendu Syndrome (OWRS), or Hereditary Hemorrhagic telangiectasia (HHT) is an autosomal dominant disease presents with epistaxis, telangiactesia and multiorgan vascular dysplasia.
Titli Bandyopadhyay
doaj   +1 more source

Rendu-Osler-Weber disease: update of medical and dental considerations

open access: yes, 2008
Rendu-Osler-Weber disease, also known as hereditary hemorrhagic telangiectasia (HHT), is an autosomal dominant inherited disorder characterized by an aberrant vascular development. The reported prevalence is approximately 1 per 5,000-10,000. The clinical
van Dijk, F. S.   +13 more
core   +1 more source

Telangiectasia hemorrágica hereditária: ácido tranexâmico no tratamento de úlcera plantar Hereditary hemorrhagic telangiectasia: tranexamic acid for plantar ulcer

open access: yesAnais Brasileiros de Dermatologia, 2005
Relato de um caso de úlcera plantar por fístula arteriovenosa em paciente portador de telangiectasia hemorrágica hereditária ou doença de Rendu-Osler-Weber tratado com ácido tranexâmico.
Gabriella Corrêa de Albuquerque   +4 more
doaj   +1 more source

Endoscopic Classification of Severe Spontaneous Epistaxis: A Case‐Series of 445 Patients

open access: yesLaryngoscope Investigative Otolaryngology, Volume 11, Issue 2, April 2026.
Epistaxis can be related to several histopathological findings. ABSTRACT Objective To identify the anatomical location and characterize the histopathological findings of severe spontaneous epistaxis through endoscopic evaluation and tissue biopsy.
Wen Zhang   +2 more
wiley   +1 more source

[Rendu-Osler-Weber disease] [PDF]

open access: yes, 2005
Contains fulltext : 48121.pdf (Publisher’s version ) (Open Access)Rendu-Osler-Weber disease or hereditary hemorrhagic telangiectasia (HHT) is a multisystem autosomal dominant hereditary disorder.
Sys, L.M., Hoogen, F.J.A. van den
core   +1 more source

Novel Simplified Nasal Endoscopy Grading System for Hereditary Hemorrhagic Telangiectasia Patients

open access: yesThe Laryngoscope, Volume 136, Issue 2, Page 652-657, February 2026.
We validated a novel, simplified nasal endoscopy grading system for patients with Hereditary Hemorrhagic Telangiectasia (HHT). Our grading (mild, moderate, severe) demonstrated strong correlation with Epistaxis Severity Score (ESS) and Quality of Life (QoL), and showed substantial inter‐rater reliability (ICC = 0.8).
Ethan Soudry   +4 more
wiley   +1 more source

Rendú Osler Weber Syndrome; case report

open access: yesRadiology Case Reports, 2022
Hereditary hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber disease, is a dominant autosomal disease characterized by the presence of multiple telangiectasia in skin and mucus, associated with arteriovenous malformations (AVM) of various organs ...
Oscar Manuel García Córdova, MD   +3 more
doaj   +1 more source

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