Browsing by Author "Correia, AJ"
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- A evolução do refluxo vesico-ureteral com diagnóstico perinatalPublication . Leitão, H; Correia, AJ; Gomes, C; Simões, O; Rolo, V; Mimoso, G; Ramos, C
- Fetopatia pelo uso de inibidores da enzima de conversão da angiotensinaPublication . Neves, S; Santos, R; Gomes, C; Correia, AJAngiotensin Converting Enzyme Inhibitors (ACEI) are commonly used antihypertensive drugs, although contraindicated during pregnancy by fetopathy association such as renal dysgenesis, oligohydramnios, hipocalvaria, pulmonary hypoplasia, intrauterine growth restriction, and neonatal anuric renal failure. The authors present a clinical report of a child that developed neonatal anuric renal failure with peritoneal dialysis support by an in uterus exposure to ACEI with very good recovery. This case and literature review states the need to avoid ACEI prescription to Young women and it's suspension as soon as possible during pregnancy.
- MÓDULO 2 - 2º Curso de Formação para Internos 2013 - 2014:Pediatria AmbulatóriaPublication . Bento, C; Rodrigues, F; Oliveira, G; Lopes, MF; Brito, MJ; Oliva, M; Dinis, I; Correia, AJ; Soares, R; Fonseca, P; Ramos, L; Mirante, A
- MÓDULO 7 - 2º Curso de Formação para Internos 2013 - 2014:Pediatria do Ambulatório de áreas diferenciadasPublication . Correia, AJ; Bento, C; Rodrigues, F; Oliveira, G; Lopes, MF; Brito, MJ
- Schimke immuno-osseous dysplasia: case report and review of 25 patientsPublication . Saraiva, JM; Dinis, A; Resende, C; Faria, E; Gomes, C; Correia, AJ; Gil, J; Fonseca, NImmuno-osseous dysplasia is characterised by spondyloepiphyseal dysplasia, lymphopenia with defective cellular immunity, and progressive renal disease. We describe a patient with a severe form of the disease, review the features of another 24 patients, and discuss the previous classification. The differences between the two groups are not striking, and although similarities are greater between affected sibs, the same diagnosis of Schimke immuno-osseous dysplasia should apply to them all. The aetiology and physiopathology of this rare osteochondrodysplasia of presumed autosomal recessive inheritance remain unknown.