Results 61 to 70 of about 1,710,432 (174)
Neurologic Manifestation as Initial Presentation in a Case of Hereditary Haemorrhagic Telangiectasia
Clinical Medicine Insights: Case Reports, 2010 Hereditary Haemorrhagic Telangiectasia (HHT), or Osler-Weber-Rendu syndrome is an uncommon autosomal dominant multi-organ condition of vascular dysplasias.
Yeow Kwan Teo, Ai Ching Kor
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Osler-Weber-Rendu syndrome: A case report
Cumhuriyet Medical Journal, 2014 Osler-Weber-Rendu (Hereditary Hemorrhagic Telangiectasia) is an autosomal dominant disease characterized by telangiectasia on mucosa and skin and arteriovenous malformations in visceral organs. Telangiectasia on lips, tongue, ear, nasal mucosa, palmoplantar region and nail beds are typical findings in the disease.
Okan Kızılyel +4 more
openaire +2 more sources
Anaesthesia Reports, Volume 14, Issue 1, January‐June 2026.Summary 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 ...
V. Pinkert +3 more
wiley +1 more source
[Rendu-Osler-Weber disease] [PDF]
, 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
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Case Reports in Gastrointestinal Medicine, Volume 2026, Issue 1, 2026.Background Hereditary hemorrhagic telangiectasia (HHT) is a rare genetic disorder characterized by mucocutaneous and visceral telangiectasias, often leading to severe complications. This case report presents an uncommon manifestation of HHT in a 57‐year‐old Black Kenyan female with upper gastrointestinal bleeding. Given the rarity of HHT in our region,
Lavender Otom +4 more
wiley +1 more source
Rendu-Osler-Weber syndrome and ocular manifestations in hereditary hemorrhagic telangiectasia [PDF]
, 1992 The relatively rare syndrome of Rendu-Osler-Weber and the associated hemorrhagic telangiectasia present with various ocular signs, such as telangiectases of the lids, conjunctiva, and retina.
Jenisch, Daniel A
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Pulmonary arteriovenous malformation in a pediatric patient with epistaxis and hypoxemia
Radiology Case Reports, 2020 Hereditary hemorrhagic telangiectasia (HHT; also known as Osler-Weber-Rendu syndrome) is an inherited vascular disorder with a spectrum of clinical manifestations depending on lesion distribution.
Ryan W. England, MD +1 more
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Characterizing the Healthcare Utilization and Costs of Hereditary Hemorrhagic Telangiectasia
American Journal of Hematology, Volume 100, Issue 10, Page 1722-1735, October 2025.ABSTRACT Hereditary hemorrhagic telangiectasia (HHT) is the second‐most common inherited bleeding disorder worldwide, afflicting one in 4000–5000 people, and is the most morbid inherited bleeding disorder of women. HHT causes recurrent severe epistaxis, chronic gastrointestinal bleeding, heavy menstrual bleeding, and arteriovenous malformations in the ...
Hanny Al‐Samkari +5 more
wiley +1 more source
Rendu-Osler-Weber Syndrome: A Case Report [PDF]
, 2020 Hereditary hemorrhagic telangectasia (HHT) or Rendu-Osler-Weber syndrome, is a rare genetic disorder with autosomal dominance and variable penetrance. The typical findings of the disease are telangiectasias in skin and mucous membranes, and arteriovenous
Vladimir Vukomanović +3 more
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Estudio genético de pacientes diagnosticados de enfermedad de Rendu-Osler-Weber (HHT) [PDF]
, 2011 [EN] Although there are previous studies that analyze the Osler Weber Rendu disease in Spanish patients, in our work we intend to analyze from a clinical standpoint and genetic characteristics of patients followed at the Hospital Universitario de ...
Cabezón Crespo, Antonio
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