Results 41 to 50 of about 3,525 (192)
Williams Syndrome and Neonatal Cardiac Surgery for Congenital Single Ventricle
Williams syndrome (WS) is an arteriopathic derangement associated with supravalvular aortic stenosis and branch pulmonary stenosis. We describe double-outlet right ventricle with mitral atresia and aortic arch hypoplasia in an infant with WS.
Taylor E. Katt, MD +5 more
doaj +1 more source
Supravalvular aortic stenosis in William′s syndrome
We report supravalvular aortic stenosis in a 12 year old patient who presented with mental retardation, malformed teeth, broad lower lips, pectus carinatum, clinodactyly, kyphoscoliosis with symptoms of shortness of breath.
Bishav Mohan, Chander Mohan Mittal
doaj +1 more source
A hipercoagulabilidade sanguínea proporcionada na gravidez aumenta consideravelmente a incidência de trombose de valvas mecânicas. A estenose supravalvar aórtica adquirida é extremamente rara.
Ricardo Adala Benfatti +3 more
doaj +1 more source
Evaluation of Supravalvular Aortic Gradient Changes Following Inverted Y-Patch Repair
INTRODUCTION: This study presents our single institute experience regarding the patients who underwent surgical correction via inverted Y-patch repair with the diagnosis of supravalvular aortic stenosis.
Gökmen Akkaya +3 more
doaj +1 more source
Surgical treatment of Shone’s syndrome and patent ductus arteriosus in an adult
Background Shone’s syndrome is a rare complex congenital anomaly. The classical definition consists of four anomalies: supravalvular mitral membrane, parachute mitral valve (PMV), subaortic stenosis, and coarctation of the aorta (CoA).
Yanzhong He +4 more
doaj +1 more source
Aortic stenosis occurs when the heart's aortic valve narrows. This narrowing prevents the valve from opening fully, which obstructs blood flow from the heart into the aorta and onward to the rest of the body.
Aso Faeq Salih
doaj +1 more source
Diffuse hypoplasia of the aortic arch and isthmus in a patient with Williams syndrome
Williams syndrome is a rare neurodevelopmental disorder characterized by mental retardation, growth deficiency, hypercalcemia, cardiac defects, and a distinctive facial appearance.
İsmihan Selen Onan +4 more
doaj +1 more source
A Case Report of the Shone Syndrome in Association with Coronary Abnormality
Shone syndrome or complex is defined by sequential left-sided heart stenosis, including supravalvular mitral membrane, valvular mitral stenosis (MS) by a parachute mitral valve, subaortic stenosis, and aortic coarctation. It is a rare entity which occurs
Shahin Rahimi +4 more
doaj +1 more source
Background: The aorto-left ventricular tunnel (ALVT) is a congenital extracardiac channel that connects the ascending aorta to the left ventricle. Case Description: A 2-year-old Shih-tzu dog presented with mild exercise intolerance.
Daji Noh +5 more
doaj +1 more source
Computerized tomography use in Williams–Beuren syndrome aortopathy
Williams–Beuren syndrome is a multisystem genetic disorder caused by hemizygous deletion on chromosome 7q11.23, encompassing about 28 genes including the elastin gene, ELN.
Neale Nicola Kalis +3 more
doaj +1 more source

