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http://dx.doi.org/10.1136/archdischild-2017-314517 | DOI Listing |
Biomed Hub
December 2024
Division of Paediatric Cardiology, Department of Paediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Centre (LUMC), Leiden, The Netherlands.
Introduction: Transposition of the great arteries (TGA), especially with intact ventricular septum (TGA-IVS), presents unique challenges during fetal-to-neonatal transition, which can contribute to developing persistent pulmonary hypertension of the newborn (PPHN).
Case Presentation: A male newborn with TGA-IVS, delivered via caesarean section, presented with hypoxemia and tachycardia immediately after birth (preductal SpO: 50-60%, post-ductal SpO: 70-75%). Echocardiography revealed a floppy interatrial septum and two interatrial connections with bidirectional shunting.
Neuropsychopharmacol Rep
December 2024
Department of Psychiatry, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.
Int J Pediatr Otorhinolaryngol
August 2024
Department of Otorhinolaryngology, Head and Neck Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea. Electronic address:
J Pak Med Assoc
June 2024
Isra Postgraduate Institute of Ophthalmology, Karachi, Pakistan.
Ned Tijdschr Geneeskd
May 2024
Radboudumc/Amalia Kinderziekenhuis, afd. Kindergeneeskunde/Expertisecentrum Prader-Willi-syndroom, Nijmegen.
Due to its rare nature and subtle dysmorphisms, Prader-Willi syndrome can be challenging to recognize and diagnose in the neonatal period. Feeding difficulties and hypotonia ('floppy infant') are the most striking characteristics. Prader-Willi syndrome requires specific follow-up and treatment, emphasizing the importance of early recognition.
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