PDF] Patent Ductus Arteriousus Device Closure in an Infant with Rubinstein–Taybi Syndrome
Por um escritor misterioso
Last updated 20 junho 2024
A typical six-month-old girl with Rubinstein–Taybi syndrome was presented with typical facial changes including downward-sloping palpebral fissures, prominent forehead, hypertelorism, limited mouth opening, large beaked nose, and high arched palate. Rubinstein–Taybi syndrome (RTS) was first described by Michail et al[1] and subsequently by Rubinstein and Taybi[2]. We present a typical six-month-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.
Pediatric Cardiothoracic Surgery - Patent Ductus Arteriosus
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Transcatheter closure of patent ductus arteriosus in a tiniest baby – 510 grams - ScienceDirect
PDF) Patent Ductus Arteriousus Device Closure in an Infant with Rubinstein–Taybi Syndrome
PDF] Patent Ductus Arteriosus Closure in Prematurities Weighing Less than 1 Kg by Subaxillary Mini-thoracotomy
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Bedside surgical ligation of the patent ductus arteriosus in very‐low‐birth‐weight premature infants: Limited upper ministernotomy as an alternative approach - Akyuz - 2021 - Journal of Cardiac Surgery - Wiley Online Library
Definitive Closure of the Patent Ductus Arteriosus in Preterm Infants and Subsequent Short-Term Respiratory Outcomes
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