Articles Related to Choanal atresia
Bilateral choanal atresia is a rare congenital malformation, which causes asphyxia neonatorum rarely compatible with life, making this pathology a diagnostic and therapeutic emergency. We report a very rare case of bilateral choanal atresia in a girl who survived to the age of 6 without neonatal care, and we discuss the clinical, endoscopic, radiological aspects and the treatment of this condition
The Health Improvement Network (THIN) provided data from UK General Practitioners (GPs) for 144 pregnant women who were prescribed zanamivir and 144 age- and date-matched untreated comparators with no recorded diagnosis of influenza. Groups were assessed for baseline characteristics, treatment-emergent diagnoses in the mother, pregnancy outcomes and congenital malformations diagnosed in the offspring within 28 days of birth.