Results 1 to 10 of about 271 (119)
Síndrome de Klippel-Trenaunay-Parkes-Weber com angiomatose medular
Arquivos De Neuro-Psiquiatria, 1975 É relatado um caso de síndrome de Klippel-Trénaunay-Parkes-Weber associada a angiomatose medular. O autor salienta ter encontrado na literatura somente uma referência com tal associação.
James Pitágoras De Mattos +1 more
exaly +4 more sources
Le syndrome Sturge-Weber: à propos d´un cas [PDF]
The Pan African Medical Journal, 2020 Le syndrome de Sturge-Weber (SWS) ou angiomatose encéphalo-faciale, est un syndrome neuro-cutané et oculaire congénital rare. Il comporte deux types de malformations: capillaire faciale congénitale à type d´angiome plan et capillaro-veineux lepto-méningé
Meriem Doumiri +5 more
doaj +2 more sources
Syndrome de Bean chez l'enfant: à propos de deux cas [PDF]
The Pan African Medical Journal, 2017 L'angiomatose diffuse ou syndrome de Bean est une entité rare caractérisée par des malformations veineuses essentiellement cutanées et digestives pouvant se compliquer d'hémorragie de gravité variable.
Achraf El Bakkaly +4 more
doaj +2 more sources
Syndrome de Sturge Weber associé au glaucome: à propos d'un cas [PDF]
The Pan African Medical Journal, 2014 Nous rapportons le cas d'un patient de 20 ans, sans antécédent pathologique particulier, qui présente depuis la naissance un angiome cutané facial, une baisse de l'acuité visuelle depuis 3 ans ainsi qu'une exophtalmie d'installation progressive de l'éil ...
Fatima Zohra El Meriague, Rajae Daoudi
doaj +2 more sources
HIV medicine for dermatologists and venereologists
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 19, Issue 1, Page 82-96, January 2021., 2021 Summary Broad administration of combined antiretroviral therapy (ART) has dramatically reduced the morbidity and mortality of the HIV‐infection and substantially improved the life expectancy of people living with HIV (PLWH). PLWH, who are effectively treated with an ART, are considered to be unable to transmit HIV.
Stefan Esser, Stefanie Sammet
wiley +1 more source
Arquivos de Neuro-Psiquiatria, 1995 The authors present the autopsy findings of two related patients and the biopsy findings of a thrid member of the family. The oldest member was 34 years old at death and on postmortem examination he had haemangioblastomas in the retina, cerebellum ...
Luiz F. Bleggi-Torres +4 more
doaj +1 more source
Brazilian Journal of Infectious Diseases, 2023 Introdução: O gênero Bartonella é constituído por bactérias reemergentes e negligenciadas. A Bartonella henselae é a espécie mais associada a doenças humanas e pode causar bacteremia assintomática, febre de origem indeterminada e vasculites, além de ...
Allisson Daniel de Carvalho Gusmão +5 more
doaj +1 more source
Bacillary angiomatosis in HIV-positive patient from Northeastern Brazil: a case report
Revista da Sociedade Brasileira de Medicina Tropical, 2011 It is a report of disseminated bacillary angiomatosis (BA) in a 23-year-old female patient, who is HIV-positive and with fever, weight loss, hepatomegaly, ascites, and papular-nodular skin lesions. The clinical and diagnostic aspects involved in the case
Renata Félix da Justa +8 more
doaj +1 more source
, 2020 JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 18, Issue 12, Page 1475-1477, December 2020.
Lukas Trennheuser +4 more
wiley +1 more source
Clinical and molecular characteristics of East Asian patients with von Hippel–Lindau syndrome
Cancer Communications, Volume 35, Issue 1, Page 1-6, December 2016., 2016 Abstract Background Von Hippel–Lindau (VHL) syndrome is a dominantly inherited multisystem cancer syndrome caused by a heterozygous mutation in the VHL tumor suppressor gene. Previous studies suggested that similar populations of Caucasian and Japanese patients have similar genotype or phenotype characteristics.
Meihua Wong +6 more
wiley +1 more source