Results 1 to 10 of about 2,601,985 (258)

Malrotation and Midgut Volvulus in Children: Diagnostic Approach, Imaging Findings, and Pitfalls

open access: yesJournal of the Korean Society of Radiology
Malrotation and midgut volvulus are surgical emergencies that commonly occur within the first month of life. The classic symptom is acute bilious vomiting, while nonspecific symptoms such as recurrent abdominal pain may be present in older children ...
Jeongju Kim   +3 more
doaj   +1 more source

Síndrome de Prune Belly

open access: yesRevista do Colégio Brasileiro de Cirurgiões
Prune Belly Syndrome is a fetal uropathy of unknown etiology with incidence of 1/35000 to 1/50000 alive been born, characterized by a classical triad: abdominal musculature congenital deficiency, bilateral criptorquidia and urinary tract malformations ...
Roni Leonardo Teixeira   +2 more
doaj   +1 more source

Neonatal screening: 9% of children with filter paper thyroid‐stimulating hormone levels between 5 and 10 μIU/mL have congenital hypothyroidism

open access: yesJornal de Pediatria (Versão em Português), 2017
Objectives: To determine the prevalence of congenital hypothyroidism in children with filter paper TSH levels (f‐TSH) between 5 and 10 μUI/mL in the neonatal screening. Methods: This was a retrospective study including children screened from 2003 to 2010,
Flávia C. Christensen‐Adad   +7 more
doaj   +1 more source

A Newborn Case of “c” Subgroup Mismatch Presenting with Severe Hemolysis and Anemia

open access: yesJournal of Pediatric Research, 2017
Hemolysis and jaundice related to Rh incompatibility in the neonatal period has decreased substantially due to the widespread use of anti-D gammaglobulin in recent years.
Ezgi Yangın Ergon   +5 more
doaj   +1 more source

Infant Mortality in Novo Hamburgo: Associated Factors and Cardiovascular Causes

open access: yesArquivos Brasileiros de Cardiologia, 2015
Background: Infant mortality has decreased in Brazil, but remains high as compared to that of other developing countries. In 2010, the Rio Grande do Sul state had the lowest infant mortality rate in Brazil.
Camila de Andrade Brum   +2 more
doaj   +1 more source

Neonatal Graves' Disease with Maternal Hypothyroidism

open access: yesAmerican Journal of Perinatology Reports, 2017
Neonatal Graves' disease presenting as conjugated hyperbilirubinemia is a diagnostic challenge because the differential includes a gamut of liver and systemic diseases.
Gangaram Akangire   +5 more
doaj   +1 more source

Progress in research on safety of vaccination in pregnancy: a review of the literature

open access: yesZhongguo gonggong weisheng
Pregnant women are a high-risk group for several infectious diseases. Vaccination is the most economical and effective way to prevent infectious diseases in the general population, but for pregnant women, vaccination can present both risks and benefits ...
Xinan NING   +3 more
doaj   +1 more source

The Study of Pulmonary Complication of Neonatal Mechanical Ventilation in NICU

open access: yesپزشکی بالینی ابن سینا, 2016
Introduction & Objective: The main indication of mechanical ventilation is in the treatment of neonates with respiratory failure. With the increased use of mechanical ventilation, its complications have increased too.
Mohammad Kazem Sabzeie   +4 more
doaj  

Espectro óculo-aurículo-vertebral em pacientes com defeitos cardíacos congênitos Espectro óculo-aurículo-vertebral en pacientes con defectos cardíacos congénitos Oculo-auriculo-vertebral spectrum in patients with congenital heart defects

open access: yesArquivos Brasileiros de Cardiologia, 2010
FUNDAMENTO: Há poucos estudos avaliando a frequência do espectro óculo-aurículo-vertebral (EOAV) nos pacientes com defeitos cardíacos congênitos (DCC). OBJETIVO: Verificar a frequência do EOAV em uma amostra de pacientes com malformações cardíacas graves.
Rafael Fabiano Machado Rosa   +7 more
doaj  

Unmasking Incontinentia Pigmenti: A Multimodal Clinico-Dermoscopic and Pathologic Correlation

open access: yesDiagnostics
Incontinentia pigmenti (IP) is a rare, X-linked dominant genodermatosis caused by mutations in the IKBKG gene and characterized by sequential cutaneous stages following the lines of Blaschko.
Michał Niedźwiedź   +3 more
doaj   +1 more source

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