Anais Brasileiros de Dermatologia, 2014 Rendu-Osler-Weber Syndrome also known as Hereditary Hemorrhagic Telangiectasia is a rare systemic fibrovascular dysplasia, with dominant autosomal inheritance.
Sheila Itamara Ferreira do Couto Meireles +4 more
doaj +1 more source
Rendu-Osler-Weber Disease [PDF]
Circulation, 2001 A 75-year-old man was admitted to the hospital because of transient unconsciousness and dysarthria. Brain CT and MRI demonstrated a recent cerebellar infarction. Physical examination revealed a continuous extracardiac murmur maximally auscultated (Levine III) between the inner edge of the right scapula and the upper thoracic vertebrae.
H, Kataoka, O, Matsuno
openaire +2 more sources
Consequences of spine imaging associated with guideline non-adherence in a pregnant patient with hereditary haemorrhagic telangiectasia. [PDF]
Anaesth RepSummary A pregnant woman with hereditary haemorrhagic telangiectasia was referred to the obstetric anaesthetic team to determine the safety of neuraxial labour analgesia. International guidelines state that the risk of complications from spinal vascular malformations during neuraxial procedures is theoretical and recommend against routine imaging of ...
Pinkert V +3 more
europepmc +2 more sources
Local sclerotherapy with Polydocanol (Aethoxysklerol®) for the treatment of Epistaxis in Rendu-Osler-Weber or Hereditary Hemorrhagic Telangiectasia (HHT): 15 years of experience* [PDF]
, 2012 Producción CientíficaHereditary Haemorrhagic Telangiectasia or Rendu-Osler-Weber syndrome is a rare autosomal dominant vascular disease characterized by mucocutaneous and gastrointestinal telangiectases and localized arteriovenous malformations in lung ...
Almaraz Gómez, Ana +4 more
core +2 more sources
Journal of Medical Sciences, 2015 Osler-Weber-Rendu syndrome is a hereditary disease which is diagnosed by criterions of clinical symptoms and examinations. Here, we report a definite case of Osler-Weber-Rendu syndrome who had epistaxis, skin telangiectasia, and pulmonary arteriovenous ...
Kuan-Yu Wang, Jen-Chih Chen, Jane-Yi Hsu
doaj +1 more source
The UK prevalence of hereditary haemorrhagic telangiectasia and its association with sex, socioeconomic status and region of residence: a population-based study [PDF]
, 2014 Background Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic disorder of aberrant blood vessel development characterised by arteriovenous malformations.
A W Fogarty +36 more
core +2 more sources
Die hereditäre hemorrhagische Telangiektasie: Untersuchungen zur Multiorganbeteiligung bei Patienten mit Epistaxis als Leitsymptom [PDF]
, 2004 Die hereditäre hämorrhagische Telangiektasie (Morbus Rendu-Osler-Weber) ist ein autosomal-dominant vererbtes vaskuläres Fehlbildungssyndrom. Hierbei werden multiple arteriovenöse Malformationen (AVM) im Bereich der Schleimhaut der oberen ...
Cerra Wollstein, Ana +1 more
core +1 more source
Clinical Case Reports, 2023 Osler‐Weber‐Rendu syndrome is an uncommon vascular disorder inherited as an autosomal dominant trait with varying penetrance and expression. A multidisciplinary approach is used for a detailed diagnostic workup and management based on the patient's ...
Sulav Pyakurel +7 more
doaj +1 more source
Osler-Weber-Rendu disease: A rare cause of recurrent hemoptysis
Lung India, 2016 Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant condition causing systemic fibrovascular dysplasia. It has an incidence of 1-2/100,000. Phenotypic variation is extreme ranging from asymptomatic
Amir M Khoja +3 more
doaj +1 more source
Mutation affecting the proximal promoter of Endoglin as the origin of hereditary hemorrhagic telangiectasia type 1 [PDF]
, 2017 [Background] Hereditary hemorrhagic telangiectasia (HHT) is a vascular multi-organ system disorder. Its diagnostic criteria include epistaxis, telangiectases in mucocutaneous sites, arteriovenous malformations (AVMs), and familial ...
Albiñana, Virginia +7 more
core +3 more sources