An extremely rare case of prenatally diagnosed absent both aortic and pulmonary valves.
Hyeon Kyeong YeonMi-Young LeeSun-Young YoonHee Jung JungJi Eun ParkJae-Yoon ShimHye-Sung WonPil-Ryang LeeAhm KimPublished in: Obstetrics & gynecology science (2016)
We describe a case of absent aortic and pulmonary valves, diagnosed at 16.4 weeks of gestation. Fetal echocardiography showed cardiomegaly with dilated both ventricles. No valve leaflets were observed in the aorta and pulmonary artery, and a typical to-and-fro flow pattern was noted in both great arteries on color Doppler imaging. Fetal hydrops was also detected. Follow-up ultrasonographic evaluation at 19 weeks demonstrated intrauterine fetal death. Postmortem autopsy revealed the absence of both aortic and pulmonary valve leaflets. To the best of our knowledge, this is the earliest diagnosed case of absent both aortic and pulmonary valves and only the second case to be diagnosed prenatally.
Keyphrases
- aortic valve
- pulmonary hypertension
- pulmonary artery
- transcatheter aortic valve replacement
- aortic valve replacement
- aortic stenosis
- pulmonary arterial hypertension
- transcatheter aortic valve implantation
- rare case
- coronary artery
- healthcare
- gestational age
- high resolution
- left ventricular
- computed tomography
- single cell
- coronary artery disease
- preterm birth
- optic nerve