Results 21 to 30 of about 8,801 (261)
Impact of Periodontal Therapy in Patients with Sturge-Weber Syndrome [PDF]
A 19 years old female patient, presented with the chief complaint of pain and swelling on her face. At physical examination, facial asymmetry and “port wine” spots on the left face were seen.
Iasminy Soares De Oliveira +4 more
doaj +1 more source
Obscure Overt Gastrointestinal Bleeding Due To Isolated Small Bowel Angiomatosis [PDF]
Isolated small bowel angiomatosis is a rare entity with a distinctive endoscopic appearance. A multidisciplinary approach is often required to diagnose and treat these complex lesions.
Chiorean, Michael V. +3 more
core +2 more sources
Skin manifestations of Bartonella infections. [PDF]
peer ...
Arrese Estrada, Jorge +2 more
core +1 more source
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
Multilocular subcutaneous bacillary angiomatosis as a primary manifestation of AIDS. [PDF]
Duckwitz TM, Yazdi AS, Kluwig D.
europepmc +3 more sources
Bacillary Angiomatosis by Bartonella Quintana in an HIV-Infected Patient [PDF]
Bacillary angiomatosis and bacillary peliosis are opportunistic infections caused by Bartonella henselae and Bartonella quintana, which occur in patients with late-stage infection.
Afonso, A +8 more
core +1 more source
Diffuse Dermal Angiomatosis Manifestation of Underlying Severe Peripheral Vascular Disease
Diffuse dermal angiomatosis is a benign vascular disorder suspected in patients with cardiovascular risk factors. We report the case of a 62-year-old woman with a non-healing hip wound but no significant cardiovascular risk factors, who was found to have
Abu Baker Sheikh +2 more
doaj +1 more source
Phenotypic Spectrum of GNA11 R183C Mosaicism. [PDF]
ABSTRACT Background Many vascular anomalies harbor postzygotic somatic variants in GNAQ and GNA11; however, the phenotype of specific G‐protein variants has not been well described. We report the clinical characteristics of 17 patients with a GNA11 R183C variant.
Zhang D +12 more
europepmc +2 more sources
Síndrome de Sturge-Weber: revisión de la literatura
El síndrome de Sturge-Weber es un trastorno neurocutáneo, congénito, esporádico e infrecuente que afecta aproximadamente a 1 de cada 20 000 a 50 0000 nacidos vivos y que se relaciona con una mutación genética activadora somática en GNAQ.
Gabriela Antezana Llaveta +1 more
doaj +1 more source
Nasu-Hakola disease (PLOSL) : report of five cases and review of the literature [PDF]
The combination of bilateral lytic lesions in the bones of the lower and upper extremities and presenile dementia is characteristic of polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, also known as Nasu-Hakola disease.
Freyschmidt, Jürgen +3 more
core +2 more sources

