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Information Journal Paper

Title

PATENT DUCTUS ARTERIOUSUS DEVICE CLOSURE IN AN INFANT WITH RUBINSTEIN–TAYBI SYNDROME (LETTERS TO EDITOR)

Pages

  708-709

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.

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  • Cite

    APA: Copy

    AGHAEI MOGHADAM, EHSAN, SAYADPOUR ZANJANI, KEYHAN, & GHANDI, YAZDAN. (2013). PATENT DUCTUS ARTERIOUSUS DEVICE CLOSURE IN AN INFANT WITH RUBINSTEIN–TAYBI SYNDROME (LETTERS TO EDITOR). IRANIAN JOURNAL OF PEDIATRICS, 23(6), 708-709. SID. https://sid.ir/paper/669184/en

    Vancouver: Copy

    AGHAEI MOGHADAM EHSAN, SAYADPOUR ZANJANI KEYHAN, GHANDI YAZDAN. PATENT DUCTUS ARTERIOUSUS DEVICE CLOSURE IN AN INFANT WITH RUBINSTEIN–TAYBI SYNDROME (LETTERS TO EDITOR). IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2013;23(6):708-709. Available from: https://sid.ir/paper/669184/en

    IEEE: Copy

    EHSAN AGHAEI MOGHADAM, KEYHAN SAYADPOUR ZANJANI, and YAZDAN GHANDI, “PATENT DUCTUS ARTERIOUSUS DEVICE CLOSURE IN AN INFANT WITH RUBINSTEIN–TAYBI SYNDROME (LETTERS TO EDITOR),” IRANIAN JOURNAL OF PEDIATRICS, vol. 23, no. 6, pp. 708–709, 2013, [Online]. Available: https://sid.ir/paper/669184/en

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