منابع مشابه
Lupus eritematoso neonatal: reporte de cuatro casos
Neonatal lupus erythematosus is a very rare disease, clinically characterized by skin lesions that resemble those of subacute or discoid lupus erythematosus and/or congenital heart block. Generally, when patients have skin manifestations, they have no cardiac defects and vice-versa; however, in 10% of cases these manifestations may coexist. Other findings may include hematologic, hepatic and ne...
متن کاملDescompresión microvascular en neuralgia del trigémino: Reporte de 36 casos y revisión de la literatura
BACKGROUND The aim of this study is to describe the results of 36 patients with trigeminal neuralgia treated with microvascular decompression. METHODS Between June 2005 and May 2012, 36 patients with trigeminal neuralgia were operated by the first author (AC), underwent microvascular decompression. The age, sex, duration of symptoms before surgery, and surgical finds, were all evaluated. In a...
متن کاملBifid Condylar Process: Cases Report Proceso Condilar Bífido. Reporte de Casos
The bifid condylar process is a rare anomaly. Most of the known cases are radiographic findings, mainly in ortopantomography and nuclear magnetic resonance. The condition is usually asymptomatic, while in some cases are associated with ankylosis of the temporomandibular joint. It is reported that the presence of bifid condylar process is not determined by age and gender, but the findings are am...
متن کاملSíndrome de Sweet: estudo de 23 casos
BACKGROUND: Sweet's syndrome or acute febrile neutrophilic dermatosis is a rare disease characterized by painful violaceous erythematous skin lesions, fever, neutrophilic leukocytosis and dense dermal neutrophilic inflammatory infiltrate. It shows excellent response to corticosteroids. OBJECTIVES: To assess cases of Sweet's syndrome in a university hospital, identifying its clinical, laboratory...
متن کاملSíndrome de Kindler - relato de dois casos
Kindler syndrome is a rare autosomal recessive genodermatosis characterized by trauma-induced blisters, progressive poikiloderma and varying degrees of photosensitivity. In 2003, loss-of-function mutations were identified in the gene KIND1 mapped to chromosome 20p12.3. In this paper, we report Kindler syndrome in two children born to consanguineous parents presenting acral blistering, photosens...
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ژورنال
عنوان ژورنال: Acta Pediátrica Hondureña
سال: 2019
ISSN: 2411-6270,2410-1400
DOI: 10.5377/pediatrica.v7i1.6936