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A case of laryngeal atresia accompanied by persistent pharyngotracheal ductus
Levent Korkmaz1, Işın Güneş2, Hülya Halis1
1Division of Neonatology, Department of Pediatrics, Erciyes University, Faculty of Medicine, Kayseri, Turkey.
Insights
Laryngeal atresia, a rare congenital anomaly, is often fatal. This case highlights a newborn with laryngeal atresia temporarily supported by partial ventilation through a persistent pharyngotracheal duct.
Area of Science:
- Neonatal Medicine
- Congenital Anomalies
- Pediatric Surgery
Background:
- Laryngeal atresia is a rare, often fatal congenital anomaly affecting 1 in 50,000 births.
- It presents with multifactorial inheritance and characteristic fetal abnormalities including dilated trachea and hydrops fetalis.
- Diagnosis is typically challenging, often identified postnatally due to respiratory distress and failed intubation attempts.
Observation:
- A rare case of a newborn diagnosed with laryngeal atresia is presented.
- The neonate experienced severe respiratory distress at birth.
- Temporary respiratory support was achieved via partial ventilation through a persistent pharyngotracheal duct.
Findings:
- This case demonstrates a rare congenital presentation of laryngeal atresia.
- Partial ventilation through a persistent pharyngotracheal duct provided initial life support.
- The condition ultimately proved fatal, underscoring the severity of laryngeal atresia.
Implications:
- Highlights the critical importance of recognizing rare congenital airway anomalies.
- Suggests potential, albeit temporary, management strategies in extreme neonatal emergencies.
- Emphasizes the need for increased physician awareness regarding laryngeal atresia and its fatal outcomes.
Abstract:
Laryngeal atresia is generally a fatal congenital anomaly with an incidence of 1: 50,000 births. This congenital anomaly is a condition of multifactorial inheritance, in which the fetus has a dilated trachea, enlarged echogenic lungs, an inverted or flattened diaphragm, fetal hydrops, and ascites. Diagnosis is usually made when there is failure to perform endotracheal intubation in a neonate with severe respiratory distress and absence of audible cry. Here, we present a very rare case of a newborn with laryngeal atresia who had respiratory distress and was sustained for the first few minutes of life using partial ventilation via a persistent pharyngotracheal duct. We would like to draw the attention of all physicians to this issue by reporting a rare fatal case of a newborn with a congenital presentation.
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