Results 41 to 50 of about 9,783 (206)

Retinal telangiectasia-like lesions in a 15-year-old female with Hereditary hemorrhagic telangiectasia – a case report

BMC Ophthalmology, 2022
Background Hereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome is a bleeding disorder that can affect all parts of the body including the eyes.
Ardiana Ala, Torben Lykke Sørensen, Caroline Schmidt Laugesen   +2 more
doaj   +1 more source

Screening pulmonary arteriovenous malformations in a large cohort of Spanish patients with hemorrhagic hereditary telangiectasia [PDF]

, 2016
39 p.-1 fig.-7 tab.Background and objectives Because of the serious nature of potential complications, screening for pulmonary arteriovenous malformations is required in patients with hereditary hemorrhagic telangiectasia.
Bernabéu, Carmelo, Botella, Luisa María, Bueno, Jesús, Cuesta, José María, Fariñas-Álvarez, Concepción, Marqués, Sarah, Parra, José A., Parra-Fariñas, Carmen, Zarauza, Jesús, Zarrabeitia, Roberto   +9 more
core   +1 more source

Oral Cryptococcosis due to Naganishia diffluens in a Patient With Thalassemia: A Case Report and a Literature Review

Journal of Clinical Laboratory Analysis, EarlyView.
Naganishia diffluens, a rare non‐neoformans cryptococcal species, was identified by PCR sequencing as the causative agent of oral cryptococcosis in a 31‐year‐old Iranian man with β‐thalassemia. This case represents the first documented instance of oral infection by N.
Zahra Yahyazadeh, Zeynab Haseli, Javad Javidnia, Mahdi Abastabar, Eisa Nazar, Hosein Jalali, Mohamad Taghi Hedayati, Hossein Karami, Mohsen Nosratabadi, Lotfollah Davoodi, Seyyed Reza Aghili, Maryam Moazeni, Iman Haghani, Hamid Badali   +13 more
wiley   +1 more source

CLINICAL APPROACH TO HEREDITARY HEMORRHAGIC TELANGIECTASIA [PDF]

Journal of IMAB, 2013
Background: Hereditary hemorrhagic telangiectasia (HHT or Rendu-Osler-Weber disease) is a rare syndrome, inherited as an autosomal dominant trait with incidence of 1/10000.
Mary Hachmeriyan, Nikolai Sapundzhiev, Miglena Georgieva, Nataliq Dobrudjanska, Venislav Stoyanov, Dimitrina Konstantinova, Lyudmila Angelova   +6 more
doaj   +1 more source

High-Flow Vascular Malformations in Children. [PDF]

, 2020
Children can have a variety of intracranial vascular anomalies ranging from small and incidental with no clinical consequences to complex lesions that can cause substantial neurologic deficits, heart failure, or profoundly affect development. In contrast
Abla, Adib A, Braunstein, Steve, Cooke, Daniel L, Fullerton, Heather J, Gupta, Nalin, Hetts, Steven W, Kim, Helen, Morshed, Ramin A, Winkler, Ethan A   +8 more
core  

Complications and clinical outcome of hepatic artery embolisation in patients with hereditary haemorrhagic telangiectasia [PDF]

, 2012
BACKGROUND: Hepatic artery embolisation (HAE) in patients with hereditary haemorrhagic telangiectasia (HHT) is controversial because of the associated complications and unproven long-term benefit.
Ajay Chavan, B. Schmuck, Hannelore Barg-Hock, Hans Seifert, Lars Luthe, Michael Gebel, Rudolph Raab, Timm Kirchhoff   +7 more
core   +1 more source

Arteriovenous Malformations in Hereditary Haemorrhagic Telangiectasia

Acta Médica Portuguesa, 2014
Keywords: Arteriovenous Malformations; Telangiectasia, Hereditary Hemorrhagic; Tomography, X-Ray Computed.
Klaus Loureiro Irion, Giordano Rafael Tronco Alves   +1 more
doaj   +1 more source

Final observation of an extremely severe case of Osler-Weber-Rendu disease in teaching at the pregraduate and postgraduate stages of education and the use of current English-language Internet applications for doctors and patients

Медицина неотложных состояний, 2023
Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome, Osler-Weber-Rendu disease, etc) is diagnosed clinically according to the so called Curacao criteria, if at least three of four of them are present: recurrent spontaneous epistaxis ...
V.M. Rudichenko, N.V. Snigir, V.О. Кrivets   +2 more
doaj   +1 more source

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, Botella, Luisa M., Millás, Teresa, Morais Pérez, Darío, Zarrabeitia Puente, Roberto   +4 more
core   +2 more sources

Nail Disorders in Systemic Conditions

JEADV Clinical Practice, EarlyView.
ABSTRACT Nail findings in children can be indicative of an underlying systemic disease. Many of these findings are seen in multiple entities and are not specific to one disease. The importance of specifically examining for these nail changes cannot be overstated.
Jane Sanders Bellet
wiley   +1 more source