Record number :
2444536
Title of article :
Patent Ductus Arteriousus Device Closure in an Infant with Rubinstein–Taybi Syndrome
Author/Authors :
Aghaei-Moghadam, Ehsan Department of Pediatric Cardiology - Tehran University of Medical Sciences , Sayadpour Zanjani, Keyhan Department of Pediatric Cardiology - Tehran University of Medical Sciences , Ghandi, Yazdan Department of Pediatric Cardiology - Tehran University of Medical Sciences
Pages :
2
From page :
708
To page :
709
Abstract :
Rubinstein–Taybi syndrome (RTS) was first described by Michail et al[1] and subsequently by Rubinstein and Taybi[2]. We present a typical sixmonth-old girl with RTS. Her mother had ovarian cancer and polyhydramnios during the pregnancy. Parents are closely related. There were frequent respiratory infections resulting in two hospital admissions. Physical examination revealed typical facial changes including downward-sloping palpebral fissures, prominent forehead, hypertelorism, limited mouth opening, large beaked nose, and high arched palate (Fig. 1). A history of increased tearing was compatible with nasolacrimal duct obstruction. Other features include general hypotonia with delayed developmental milestones, short and broad thumbs and toes (Fig. 1). Chest x-ray showed cardiomegaly (Fig. 2). She had normal karyotype. A continuous murmur was auscultable in the left upper parasternal region. Echocardiography showed a patent ductus arteriousus (PDA). Angiography confirmed a type E PDA with narrowest and aortic diameters of 3 and 6 mm, respectively. Systolic pressure in pulmonary artery was 45 mmHg. The PDA was closed with a detachable Cook coil 6.5×4 (William Cook Europe, Denmark). A small residue remained which decreased two weeks later on another echocardiogram. RTS is sporadic with a birth prevalence of 1 in 100000 to 125000[3,4]. Both sexes are equally affected[5]. Typical facial expression (comical face) includes downward sloping palpebral fissures, hypertelorism, large beaked nose, malpositioned ears, limited mouth opening, long eye lashes, high arched eyebrows and hirsutism[6]. Skeletal features consist of short stature, broad and deviated thumbs, broad toes, pes planus and scoliosis. Cardiac involvement occurs in about 36%, mostly as atrial or ventricular septal defects, PDA, coarctation of aorta, pulmonic stenosis and bicuspid aortic valve[7].
Keywords :
Coil Closure , Rubinstein–Taybi Syndrome , Patent Ductus Arteriosus
Journal title :
Astroparticle Physics
Serial Year :
2013
Link To Document :
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