OAR@UM Community:/library/oar/handle/123456789/274832025-11-13T21:40:16Z2025-11-13T21:40:16ZPulmonary valvulotomy in a fetus with pulmonary atresia with intact ventricular septum : first experience in TurkeyPolat, Tugcin BoraDanısman, N./library/oar/handle/123456789/43002020-07-03T11:25:00Z2012-01-01T00:00:00ZTitle: 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.2012-01-01T00:00:00ZSpontaneous subarachnoid haemorrhage due to coarctation of aorta and intraspinal collaterals : a rare presentationDevara, Anil K.V.Joseph, S.Uppu, S.C./library/oar/handle/123456789/42992018-06-11T12:43:36Z2012-01-01T00:00:00ZTitle: Spontaneous subarachnoid haemorrhage due to coarctation of aorta and intraspinal collaterals : a rare presentation
Authors: Devara, Anil K.V.; Joseph, S.; Uppu, S.C.
Abstract: The occurrence of spontaneous subarachnoid haemorrhage (SAH) in association with coarctation of
thoracic aorta and absence of intracranial aneurysm is a rare association. In spontaneous SAH, the
predominant cause is intracranial aneurysmal rupture. This report describes a case of a 40 year-old
male who presented with SAH and was incidentally diagnosed to have coarctation of aorta (CoA)
with intraspinal collaterals on further work up. This case demonstrates the importance of detailed
evaluation of patients with spontaneous SAH on whom common aetiologies have been ruled out.2012-01-01T00:00:00ZPacemaker-associated cyanosis in an adolescent : the answer hiding behind shadowsWittekind, S.G.Salerno, Jack ChristianRubio, Agustin E./library/oar/handle/123456789/42922017-12-05T10:01:42Z2012-01-01T00:00:00ZTitle: Pacemaker-associated cyanosis in an adolescent : the answer hiding behind shadows
Authors: Wittekind, S.G.; Salerno, Jack Christian; Rubio, Agustin E.
Abstract: Lead thrombosis is a recognized complication of permanent transvenous pacemaker (PM)
implantation. We present the interesting case of an adolescent with a dual-chamber PM presenting
with fatigue and hypoxemia. Due to limitations of various imaging modalities, the diagnosis was
difficult. She was eventually diagnosed with intracardiac PM lead thrombi obstructing tricuspid
valve inflow. The pediatric literature on PM lead thrombosis is also briefly reviewed.2012-01-01T00:00:00ZGastric pseudoaneurysm in the setting of Loey’s Dietz SyndromeLikes, Maggie L.Johston, Troy Alan/library/oar/handle/123456789/42852020-04-06T17:35:05Z2012-01-01T00:00:00ZTitle: 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