Results 51 to 60 of about 6,765 (189)

RENDU-OSLER-WEBER DISEASE AT 75 YEARS OLD WOMAN

Архивъ внутренней медицины, 2017
The publication presents a clinical case of hereditary hemorrhagic telangiectasia in a woman of 75 years. In the first part of the article, literature data on the incidence and features of Rundu-Osler-Weber disease are presented, modern diagnostic ...
A. S. Barmenova, T. A. Bayesheva, N. S. Umbetalina, V. A. Suhova   +3 more
doaj   +1 more source

Osler-Weber-Rendu Disease Uncovered by Preeclampsia in a Case Report

Case Reports in Obstetrics and Gynecology, 2020
Osler-Weber-Rendu disease (OWRD), called hereditary hemorrhagic telangiectasia, is an uncommon genetic illness with the dominant autosomal transmission.
Jamal Ouachaou, Hamza Mimouni, Mohammed Maarad, Yassine Mellagui, Asmae Oulad Amar, Houssam Bkiyar, Imane Kamaoui, Brahim Housni   +7 more
doaj   +1 more source

Pericytes as targets in hereditary hemorrhagic telangiectasia [PDF]

Frontiers in Genetics, 2015
Defective paracrine Transforming Growth Factor-β (TGF-β) signaling between endothelial cells and the neighboring mural cells have been thought to lead to the development of vascular lesions that are characteristic of Hereditary Hemorrhagic Telangiectasia (HHT). This review highlights recent progress in our understanding of TGF-β signaling in mural cell
Thalgott, Jérémy, Dos-Santos-Luis, Damien, Lebrin, Franck   +2 more
openaire   +3 more sources

Infective endocarditis with Osler’s nodule in a patient with Osler’s disease: a case report and review of the literature

Journal of Medical Case Reports, 2022
Background Hereditary hemorrhagic telangiectasia, also known as Osler–Weber–Rendu disease, induces arteriovenous malformations in visceral organs. Arteriovenous malformations increase the risk of severe infections and are a common complication associated
Genki Naruse, Takatomo Watanabe, Hiroyuki Okura   +2 more
doaj   +1 more source

Review of the Molecular and Developmental Basis of Myhre Syndrome, Bench Research

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MS) is a connective‐tissue disorder within the acromelic dysplasia spectrum. It is characterized by congenital craniofacial, skeletal, cutaneous anomalies, respiratory, cardiovascular along with intellectual disability, deafness, and progressive fibrosis.
Camille Viaut, Valerie Cormier‐Daire
wiley   +1 more source

Hereditary hemorrhagic telangiectasia and pregnancy: potential adverse events and pregnancy outcomes

, 2017
Omar Bari,1 Philip R Cohen2 1School of Medicine, University of California San Diego, La Jolla, CA, USA; 2Department of Dermatology, University of California San Diego, La Jolla, CA, USA Abstract: Hereditary hemorrhagic telangiectasia (HHT) is an ...
Cohen PR, Omar Bari, Bari O, Philip R Cohen   +3 more
core   +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

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

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

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