Congenital Abnormalities
Mostrando 1-12 de 350 artigos, teses e dissertações.
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1. Double-lumen Aortic Arch: Persistence of the Fifth Aortic Arch?
Abstract Double-lumen aortic arch is a rare congenital anomaly related to persistence of the fifth aortic arch. It may be found alone or in association with other anatomical changes of the heart. We report a case of double-lumen aortic arch associated with coarctation of the aorta and patent ductus arteriosus in a child with a congenital malformation known a
Int. J. Cardiovasc. Sci.. Publicado em: 2021-04
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2. Impact of the reduction in TSH cutoff level to 6 mIU/L in neonatal screening for congenital hypothyroidism in Santa Catarina: final results
ABSTRACT Oubjective: To assess the implications of changing the cutoff level of TSH from 10 to 6 mIU/L. Subjects and methods: The study population was constituted by 74.123 children screened for congenital hypothyroidism by the National Screening Program in Santa Catarina, from March 2011 to February 2012. The cutoff of TSH was 6 mIU/L. If TSH between 6-10
Arch. Endocrinol. Metab.. Publicado em: 2020-12
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3. Congenital Heart Disease Revealing Familial 22q11 Deletion Syndrome
Abstract Congenital heart defects are the most common birth defects and the leading cause of mortality in the first year of life. It is well known that the 22q11 deletion syndrome (22q11DS) is the most common microdeletion syndrome in humans and that congenial heart diseases (CHDs) are one of the most common phenotypic manifestations. However, it should be n
Int. J. Cardiovasc. Sci.. Publicado em: 2020-07
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4. Application of Cervical Vestibular-Evoked Myogenic Potentials in Adults with Moderate to Profound Sensorineural Hearing Loss: A Preliminary Study
Abstract Introduction The cochlea and the vestibular receptors are closely related in terms of anatomy and phylogeny. Patients with moderate to profound sensorineural hearing loss (MPSHL) should have their vestibular organ functions tested. Objective To evaluate the incidence of vestibular abnormalities in patients with MPSHL and to study the correlation
Int. Arch. Otorhinolaryngol.. Publicado em: 2020-03
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5. Fetal structural anomalies diagnosed during the first, second and third trimesters of pregnancy using ultrasonography: a retrospective cohort study
ABSTRACT BACKGROUND: The prevalence of congenital abnormalities in general populations is approximately 3-5%. One of the most important applications of obstetric ultrasound is in detection of fetal structural defects. OBJECTIVE: To assess fetal structural anomalies diagnosed using ultrasound in the three trimesters of pregnancy. DESIGN AND SETTING: Ret
Sao Paulo Med. J.. Publicado em: 13/01/2020
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6. Idiopathic thrombocytopenic purpura in a patient with situs inversus totalis: case report and literature review
RESUMO Situs inversus totalis é uma anormalidade congênita autossômica recessiva rara em que os órgãos mediastinais e abdominais encontram-se em posição espelhada em relação à topografia habitual. A literatura relata alguns casos de concomitância do situs inversus totalis com outras condições: anomalias espinhais, malformações cardíacas e doe
Einstein (São Paulo). Publicado em: 10/01/2020
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7. Clinical aspects of congenital microcephaly syndrome by Zika virus in a rehabilitation center for patients with microcephaly
RESUMO OBJETIVO Pretende-se, neste estudo, identificar a prevalência de variáveis clínicas em crianças com microcefalia. MÉTODOS Trata-se de um estudo transversal e observacional com dados coletados de prontuários de pacientes admitidos no ambulatório de microcefalia de um centro de referência em Teresina (PI). Foram coletados dados demográficos (
Rev. Assoc. Med. Bras.. Publicado em: 07/11/2019
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8. Embryonic malformations in an offspring of the shortnose guitarfish
ABSTRACT Embryonic malformations can be a result of exposure toxic substances (pollution), lack of nutrients, physical restraint, genetic disorders, or infections and diseases. Such malformations can be classified according to severity and offspring survival outside the uterus. Moreover, abnormalities are normally restricted to a small portion of the litter,
Braz. j. oceanogr.. Publicado em: 28/10/2019
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9. Congenital abnormalities and anatomical variations of the vermiform appendix and mesoappendix
RESUMO Objetivo: O objetivo desta revisão foi apresentar e discutir as variações anatômicas e anomalias congênitas do apêndice vermiforme e mesoapêndice relatados nos últimos anos e suas associações com apendicite aguda e outras patologias associadas. Métodos: A busca foi realizada nas seguintes bases de dados: Pubmed, Science Direct e Scielo.
J. Coloproctol. (Rio J.). Publicado em: 30/09/2019
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10. Anesthesia for surgical repair of the pentalogy of Cantrell: case report
Resumo A pentalogia de Cantrell é uma anomalia congênita associada a defeitos na formação da parede abdominal, do esterno, diafragma e pericárdio diafragmático, além do desenvolvimento de anomalias cardíacas. É uma doença rara, com incidência estimada em um caso para cada 65.000 nascimentos, mais comum no sexo masculino (60% dos casos). Apresenta
Rev. Bras. Anestesiol.. Publicado em: 12/08/2019
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11. Tendência de malformações congênitas e utilização de agrotóxicos em commodities: um estudo ecológico
RESUMO O objetivo deste artigo foi analisar a tendência de malformações congênitas e a associação entre o uso de agrotóxicos em microrregiões de estados brasileiros que possuem maior produção de commodities agrícolas. Estudo ecológico de análise temporal conduzido com informações dos nascidos vivos (Sinasc/Ministério da Saúde), elaborando-se
Saúde debate. Publicado em: 05/08/2019
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12. Descriptive study of suspected congenital Zika syndrome cases during the 2015-2016 epidemic in Brazil
Abstract INTRODUCTION: Clinical and epidemiological data on suspected congenital Zika syndrome (CZS) cases from southern Mato Grosso (MT) in Brazil during the Zika virus (ZIKV) outbreak in 2015-2016 were evaluated. METHODS: This is a descriptive case series study of newborns whose mothers were suspected cases of ZIKV infections during their pregnancies. Th
Rev. Soc. Bras. Med. Trop.. Publicado em: 18/07/2019