A recent case report from the researchers at the University of São Paulo, published in the journal CLINICS, shows how newborns can also be infected with severe acute respiratory syndrome coronavirus 2 ...
A gene change may explain why some newborn babies struggle for breath, and could lead to genetic biomarker-based tests to warn of the risk. Neonatal respiratory distress syndrome (RDS) is a breathing ...
Newborns with respiratory distress should be evaluated for primary ciliary dyskinesia, a rare genetic disease that has features similar to cystic fibrosis, says Thomas Ferkol, M.D., from Washington ...
The objective of the study was to compare thoracic fluid content (TFC) between newborn infants with and without respiratory distress. We tested the hypothesis that TFC would be higher in infants with ...
Two-term infants were diagnosed with Kartagener Syndrome in the immediate neonatal period following presentation with unexplained respiratory distress and situs inversus. This allowed early initiation ...
A 4-month-old boy presented to the emergency department (ED) with a 3-day history of rhinorrhea and cough. The night before hospitalization, his parents took him to an acute care center, where a ...
Please provide your email address to receive an email when new articles are posted on . Jennifer A. Wambach, MD, assistant professor of pediatrics at Washington University School of Medicine, St.
Some infants are more susceptible to potentially life-threatening breathing problems after birth, and rare, inherited DNA differences may explain why, according to new research. Some infants are more ...
Please provide your email address to receive an email when new articles are posted on . As prenatal PM 2.5 exposure rose, so did the odds for assisted ventilation, multiple interventions and systemic ...
THE respiratory-distress syndrome, or hyalinemembrane disease, is the commonest cause of death among newborn, especially premature, infants, and yet its pathogenesis remains a mystery and its ...
Newborns with respiratory distress should be evaluated for primary ciliary dyskinesia, a rare genetic disease that has features similar to cystic fibrosis, says Thomas Ferkol, M.D., from Washington ...
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