A Case of Prenatally Diagnosed Uhl's Anomaly with Absent Pulmonary Valve Leaflets and Dysplastic Tricuspid Valve.
Taehong KimHoon KoJoung-Hee ByunHyoung Doo LeeHyungtae KimKwangho ChoiJoo Young NaPublished in: Children (Basel, Switzerland) (2021)
Uhl's anomaly is a very rare malformation of unknown cause, characterized by complete or partial absence of the right ventricular myocardium. The cardiac malformation causes progressive right heart failure, increased right-sided cardiac pressure, massive peripheral edema, and ascites. Patients usually present in infancy and rarely survive to adulthood. Previously, diagnosis was made at post-mortem evaluation, but advances in cardiac imaging now permit diagnosis during fetal life. We report a case of Uhl's anomaly in a newborn baby imaged at 23 + 3 weeks of gestation by fetal echocardiography. There was an aneurysmally dilated thin-walled right ventricle with hypertrophy of the right ventricular apical muscles, the tricuspid valve was dysplastic, and the pulmonary valve leaflets were absent.
Keyphrases
- mitral valve
- left ventricular
- aortic stenosis
- aortic valve
- ejection fraction
- heart failure
- pulmonary hypertension
- transcatheter aortic valve replacement
- cardiac resynchronization therapy
- end stage renal disease
- multiple sclerosis
- chronic kidney disease
- depressive symptoms
- newly diagnosed
- prognostic factors
- computed tomography
- gestational age
- photodynamic therapy
- weight loss
- pulmonary arterial hypertension
- body mass index
- patient reported outcomes
- fluorescence imaging