Congenital Malformations
Mostrando 1-12 de 268 artigos, teses e dissertações.
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1. Glycemic and nonglycemic mechanisms of congenital malformations in hyperglycemic pregnancies: a narrative review
ABSTRACT Congenital malformations are more frequently found among children born to mothers with diabetes than in the background population. There are several complex mechanisms involved in the development of congenital malformations in the offspring of mothers with hyperglycemia, such as the overexpression of glucose transporters (GLUTs) 1 and 2, the increas
Archives of Endocrinology and Metabolism. Publicado em: 2022
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2. Perinatal outcomes of prenatal diagnosis of congenital pulmonary airway malformation: an experience
SUMMARY OBJECTIVE: This study aimed to assess the perinatal outcomes of pregnancies with a prenatal diagnosis of congenital cystic adenomatoid malformation. METHODS: We conducted a retrospective cohort study based on information contained in the medical records of pregnant women whose fetuses had been prenatally diagnosed with congenital cystic adenomatoid
Revista da Associação Médica Brasileira. Publicado em: 2022
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3. What do Cochrane systematic reviews say about congenital vascular anomalies and hemangiomas? A narrative review
ABSTRACT BACKGROUND: Congenital vascular anomalies and hemangiomas (CVAH) such as infantile hemangiomas, port-wine stains and brain arteriovenous malformations (AVMs) impair patients’ lives and may require treatment if complications occur. However, a great variety of treatments for those conditions exist and the best interventions remain under discussion.
Sao Paulo Medical Journal. Publicado em: 2022
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4. Morbidity and mortality due to surgical congenital malformations from the perspective of surgical neonatal ICU outside a maternity service: a retrospective cohort study
RESUMO OBJETIVO: Traçar o perfil de pacientes atendidos em uma Unidade de Terapia Intensiva Neonatal cirúrgica nível III desvinculada de maternidade e analisar fatores de risco para mortalidade nesta população. MÉTODOS: estudo de coorte retrospectivo, avaliando os pacientes internados em um serviço de Unidade de Terapia Intensiva Neonatal cirúrgica
Rev. Assoc. Med. Bras.. Publicado em: 2020-09
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5. Type II Aortopulmonary Window with Isolated Left Subclavian Artery from Left Pulmonary Artery
Abstract Type II Aortopulmonary window (APW) accounts for only 10% of total cases of APW, which by itself is a rare congenital anomaly. Various cardiac malformations have been reported to be associated with this rare anomaly. We report one such association of origin of left subclavian artery (LSCA) from left pulmonary artery (LPA) via ductus arteriosus that
Braz. J. Cardiovasc. Surg.. Publicado em: 2020-06
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6. Coarctation of The Aorta: A Case-Series from a Tertiary Care Hospital
Abstract Background: Coarctation of the aorta is a congenital segmental narrowing of the aortic arch with severe hemodynamic repercussions and increased cardiovascular mortality. Early surgical correction and life-time echocardiographic follow-up must be performed to improve prognosis. However, this goal has been challenged by high rates of underdiagnosis,
Int. J. Cardiovasc. Sci.. Publicado em: 2020-02
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7. Coarctation of the Aorta: Its Importance for Pediatricians and Cardiologists
Abstract Background: Coarctation of the aorta is a congenital segmental narrowing of the aortic arch with severe hemodynamic repercussions and increased cardiovascular mortality. Early surgical correction and life-time echocardiographic follow-up must be performed to improve prognosis. However, this goal has been challenged by high rates of underdiagnosis,
Int. J. Cardiovasc. Sci.. Publicado em: 2020-02
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8. Relationship of databases of live births and infant deaths for analysis of congenital malformations
Resumo Objetivos: descrever a prevalência das malformações congênitas em nascidos vivos no Recife, com base no relacionamento de dados de nascimentos e óbitos infantis . Métodos: estudo transversal com dados do Sistema de Informações sobre Nascidos Vivos (Sinasc) e Mortalidade (SIM) de residentes no Recife-PE, entre 2013 e 2015. Realizou-se linkage
Rev. Bras. Saude Mater. Infant.. Publicado em: 13/01/2020
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9. Type II Aortopulmonary Window with Isolated Left Subclavian Artery from Left Pulmonary Artery
Abstract Type II Aortopulmonary window (APW) accounts for only 10% of total cases of APW, which by itself is a rare congenital anomaly. Various cardiac malformations have been reported to be associated with this rare anomaly. We report one such association of origin of left subclavian artery (LSCA) from left pulmonary artery (LPA) via ductus arteriosus that
Braz. J. Cardiovasc. Surg.. Publicado em: 13/01/2020
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10. 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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11. Cattle diseases in Mato Grosso do Sul, Brazil: a 24-year survey (1995-2018)
RESUMO: Em um levantamento sobre doenças de bovinos, revisamos os protocolos de 5.083 necropsias de bovinos realizadas no período de janeiro de 1995 a dezembro de 2018 e arquivados no Laboratório de Anatomia Patológica (LAP) da Universidade Federal de Mato Grosso do Sul (UFMS). Essas necropsias foram realizadas pelos veterinários e professores do LAP-UF
Pesq. Vet. Bras.. Publicado em: 04/11/2019
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12. 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