Abstract
We report a case of a newborn with tetrasomy 18p who presents with both a congenital diaphragmatic hernia and a giant hiatal hernia. While these two hernias have been rarely reported together in the newborn period, this represents the first association with the chromosomal abnormality of tetrasomy 18p. • The association of congenital diaphragmatic hernia and hiatal hernia together has not been previously reported in a case of tetrasomy 18p. • An abdominal surgical approach may be favored for diagnosing and repairing both of these defects simultaneously.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
