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Diagnóstico pré-natalPrenatal diagnosis
(ABRASCO - Associação Brasileira de Saúde Coletiva, 2002)
Diagnóstico prenatal de ciclopía asociada con trisomía 13.
(2013-07-12)
Se presenta un caso de ciclopía con diagnóstico prenatal por ecografía bidimensional y tridimensional, a quien se le realizó
cordocentesis, el cariotipo en sangre fetal con bandeo G mostró trisomía 13 libre, las características ...
Congenital duodenal obstruction: does prenatal diagnosis improve the outcome?
(SpringerNew YorkEUA, 2004)
Predição e prevenção do crescimento intrauterino restritoPrediction and prevention of intrauterine growth restriction
(Federação Brasileira das Sociedades de Ginecologia e Obstetricia, 2015)
Prenatal Diagnosis: advances and prospectivesDiagnóstico pré-natal: avanços e perspectivas
(HCPA/FAMED/UFRGS, 2022)
Prenatal Diagnosis of Lissencephaly Type 2 using Three-dimensional Ultrasound and Fetal MRI: Case Report and Review of the Literature
(Federacao Brasileira Soc Ginecologia & Obstetricia-Febrasgo, 2016)
Lissencephaly is a genetic heterogeneous autosomal recessive disorder characterized by the classical triad: brain malformations, eye anomalies, and congenital muscular dystrophy. Prenatal diagnosis is feasible by demonstrating ...
Difficulties observed in a reference center in the diagnosis and management of pregnant women with toxoplasmosisDificuldades observadas em um centro de referência no diagnóstico e manejo de gestantes com toxoplasmose
(Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS), 2018)
Prenatal diagnosis of posterior mediastinal lymphangioma by two- and three-dimensional ultrasonography
(WILEY-BLACKWELL, 2008)
Lymphangioma is a rare benign tumor characterized by proliferating lymph vessels and composed of large cyst spaces with endothelium-lined channels of varying dimensions. The incidence of lymphangioma is approximately one ...
Case Report: A prenatal diagnosis of osteogenesis imperfecta in a patient with a novel pathogenic variant in COL1A2
(F1000 Research, 2023)
Osteogenesis imperfecta is considered a rare genetic condition which is characterized by bone fragility. In 85% of cases, it is caused by mutations in COL1A1 and COL1A2 genes which are essential to produce type I collagen. ...