Truncus Arteriosus Type 1: A Prenatal Diagnosis, Case Report, and Literature Review | Zendy

Alireza Golbabaei | Zendy; Sara Memarian | Zendy; Mahsa Naemi | Zendy; Azade Rastgar | Zendy; Rana Karimi | Zendy; Behdad Gharib | Zendy; Mohammad-Taghi Majnoon | Zendy

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Truncus Arteriosus Type 1: A Prenatal Diagnosis, Case Report, and Literature Review

Author(s) -

Alireza Golbabaei,

Sara Memarian,

Mahsa Naemi,

Azade Rastgar,

Rana Karimi,

Behdad Gharib,

Mohammad-Taghi Majnoon

Publication year - 2021

Publication title -

journal of pediatrics review

Language(s) - English

Resource type - Journals

eISSN - 2322-4401

pISSN - 2322-4398

DOI - 10.32598/jpr.9.2.880.3

Subject(s) - truncus arteriosus , truncus , cardiology , medicine , pulmonary artery , ventricular outflow tract , ductus arteriosus , trunk , fetus , heart disease , pregnancy , tetralogy of fallot , biology , ecology , genetics

Common arterial trunk (persistent truncus arteriosus) is a rare, congenital heart anomaly and characterized by Ventricular Septal Defect (VSD), single truncal valve, and a common ventricular outflow tract. We reported a case of truncus arteriosus type 1 in the fetus of a 28 years-old G2-P1-L1 pregnant female at 24 weeks of gestational age with large sub truncul VSD, truncal overriding, and main pulmonary artery bifurcation to the right and left pulmonary arteries.

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