OAR@UM Collection:
/library/oar/handle/123456789/3649
2025-11-13T11:53:36ZPulmonary valvulotomy in a fetus with pulmonary atresia with intact ventricular septum : first experience in Turkey
/library/oar/handle/123456789/4300
Title: Pulmonary valvulotomy in a fetus with pulmonary atresia with intact ventricular septum : first experience in Turkey
Authors: Polat, Tugcin Bora; Danısman, N.
Abstract: The mortality and morbidity of children with pulmonary atresia with intact ventricular septum
(PA/IVS) is closely related with right ventricle hypoplasia and its consequent hemodynamics.
Prenatal intervention for fetuses with PA/IVS has the potential to improve growth of the RV and the
prospect of a biventricular outcome after birth. Successful valvulotomy of the pulmonary valve (PV)
was performed in a fetus with PA/IVS at 28 weeks. Following the procedure there was an
improvement in fetal hemodynamics. In utero perforation and dilation of the PV in midgestation
fetuses with PA/IVS is technically feasible. The initial results are promising and may be associated
with improved right heart growth and postnatal outcome.2012-01-01T00:00:00ZGastric pseudoaneurysm in the setting of Loey’s Dietz Syndrome
/library/oar/handle/123456789/4285
Title: Gastric pseudoaneurysm in the setting of Loey’s Dietz Syndrome
Authors: Likes, Maggie L.; Johston, Troy Alan
Abstract: Loey’s Dietz syndrome is a disorder of connective tissue caused by a mutation in the genes that
encode transforming growth factor (TGF) beta receptor 1 and 2.
It is an autosomal dominant
disorder similar to Marfan’s syndrome but with a more aggressive clinical course.
Patients with
Loey’s-Dietz syndrome have progressive dilatation of the aortic root that can lead to aortic
dissection and rupture. The location of non-aortic arterial aneurysms may be wide spread but often
occur in the head and neck vessels.2012-01-01T00:00:00Z