Results 71 to 80 of about 8,263 (226)

Leber's Hereditary Optic Neuropathy: A Case Report

open access: yesKaohsiung Journal of Medical Sciences, 2003
Leber's hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disease that primarily affects the optic nerve, causing bilateral vision loss in juveniles and young adults.
Chi-Wu Chang   +2 more
doaj   +1 more source

Telangiectasia nevoide unilateral adquirida em homem hígido Acquired unilateral nevoid telangiectasia in a healthy men

open access: yesAnais Brasileiros de Dermatologia, 2010
A Telangiectasia Nevoide Unilateral é uma dermatose vascular rara, caracterizada por áreas de telangiectasia superficial, em uma distribuição linear unilateral, descrita, em 1899, por Zeisler e Blaschko. Diversas teorias foram desenvolvidas para explicar
Juliana Merheb Jordão   +3 more
doaj   +1 more source

Histopathological evaluation of seven Amazon species of freshwater ornamental armored catfish

open access: yesActa Scientiarum: Biological Sciences, 2014
Fish commonly known as acaris or plecos are freshwater armored catfish economically important as a food resource and as ornamental fish. Most of these species are captured in the Amazon region. However, despite its economic importance, there is a lack of
Rodrigo Yudi Fujimoto   +5 more
doaj   +1 more source

Coats disease

open access: yesThe Pan African Medical Journal, 2015
Coats' disease is an idiopathic ophthalmic condition caused by a defect in the development of retinal vasculature, characterized by retinal telangiectasis, haemorrhages, intraretinal and subretinal exudation.
Samar Younes, Hicham Tahri
doaj   +1 more source

Gastric telangiectasis: a rare cause of severe blood loss in CREST syndrome [PDF]

open access: bronze, 1994
Emad El‐Omar   +4 more
openalex   +1 more source

Pulmonary arteriovenous fistula in the newborn: a case report of Rendu-Osler-Weber syndrome and a review of the literature

open access: yesThe Turkish Journal of Pediatrics, 2001
In most instances, congenital arteriovenous fistula is only one manifestation of a more widespread abnormality; 60% of patients also have hereditary hemorrhagic telangiectasis (Rendu-Osler-Weber syndrome).
R Olguntürk   +5 more
doaj  

Case for diagnosis Caso para diagnóstico

open access: yesAnais Brasileiros de Dermatologia, 2013
A 27 year-old-man, with no known personal or familial history of disease, mentioned a 10-year history of asymptomatic groups of telangiectasias, with a Blaschko lines distribution on the right lateral aspect of the neck and asymptomatic.
André Lencastre   +1 more
doaj  

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