Results 11 to 20 of about 16,744 (152)
Estenose aórtica supravalvar em adulto com anomalia de vasos da base e insuficiência aórtica
A estenose aórtica supravalvar é uma rara cardiopatia congênita, bastante incomum em adultos. Apresentamos um caso de estenose aórtica supravalvar em adulto com anomalia de vasos do arco aórtico, já com presença de insuficiência aórtica importante ...
Acrisio Sales Valente +5 more
doaj +2 more sources
Implante de marcapasso em paciente com veia cava superior esquerda persistente [PDF]
A persistência da veia cava superior esquerda, embora rara, é a anomalia venosa mais encontrada no tórax, com prevalência de 0,3-0,5% na populaçao geral. Em associaçao com a cardiopatia congênita, sua prevalência aumenta para 2,8-4,3%.
Ana Paula Frederico Tótora +3 more
doaj +5 more sources
Anoftalmia bilateral como defeito congênito isolado: uma abordagem etiológica e psicossocial [PDF]
A anoftalmia é uma condição oftalmológica rara, caracterizada pela ausência de um ou ambos os olhos, de etiologia não elucidada, podendo ser congênita, adquirida ou associada a outras síndromes sistêmicas.
Diego Davi Corso +3 more
doaj +2 more sources
Liberação médico-jurídica da antecipação terapêutica do parto em anencefalia: implicações éticas
Resumo Anencefalia é anomalia congênita na qual o tubo neural fecha-se incorretamente, comprometendo a formação da abóbada craniana e de grande parte do encéfalo. Por isso considera-se, em anencefalia, a hipótese de inviabilidade fetal.
Samuel Servinhani Fernandes +3 more
doaj +2 more sources
ABSTRACT Objectives Congenital knee dislocation (CKD) is a rare condition, affecting 1 in 100 000 newborns. Its prenatal diagnosis is challenging and not well described in the literature, especially when it appears isolated and not as part of a complex malformation or syndromic pattern. The purpose of this study was to provide a comprehensive review of
P. I. Cavoretto +7 more
wiley +1 more source
Amniotic band syndrome and limb body wall complex in Europe 1980–2019
Abstract Amniotic band syndrome (ABS) and limb body wall complex (LBWC) have an overlapping phenotype of multiple congenital anomalies and their etiology is unknown. We aimed to determine the prevalence of ABS and LBWC in Europe from 1980 to 2019 and to describe the spectrum of congenital anomalies.
Jorieke E. H. Bergman +35 more
wiley +1 more source
Prevalence and mortality among children with anorectal malformation: A multi‐country analysis
Abstract Purpose We examined the total prevalence, trends in prevalence, and age‐specific mortality among individuals with anorectal malformation (ARM) Methods We conducted a retrospective cohort study using data from 24 population‐ and hospital‐based birth defects surveillance programs affiliated with the International Clearinghouse for Birth Defects ...
Vijaya Kancherla +30 more
wiley +1 more source
ABSTRACT Objectives To compare the reported rate of any congenital anomaly and perinatal outcome of pregnancy following blastocyst‐ vs cleavage‐stage embryo transfer using a pairwise meta‐analysis and to evaluate the same outcomes following fresh‐blastocyst, frozen‐blastocyst, fresh‐cleavage or frozen‐cleavage embryo transfer using a network meta ...
C. Siristatidis +6 more
wiley +1 more source
Abstract Real‐world evidence (RWE) is emerging as a fundamental component of the post‐marketing evaluation of medicinal products. Even though the focus on RWE studies has increased in Colombia, the availability of secondary data sources to perform this type of research is not well documented.
Juan‐Sebastian Franco, David Vizcaya
wiley +1 more source
Exposure to misoprostol and hormones during pregnancy and risk of congenital anomalies Exposição ao misoprostol e hormônios durante a gravidez e risco de anomalia congênita [PDF]
This study evaluated the association between use of misoprostol and other drugs to induce menstruation, and congenital anomalies. A sample of 4,856 pregnant women 20 years and older were enrolled consecutively in prenatal services in the Unified National
Tatiane da Silva Dal Pizzol +2 more
core +1 more source

