مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

SANDIFER'S SYNDROME: A MISDIAGNOSED AND MYSTERIOUS DISORDER (LETTERS TO EDITOR)

Pages

  715-716

Abstract

SANDIFER's Syndrome (SS) is a rare pediatric manifestation of gastro-esophageal reflux (GER) disease characterized by abnormal and dystonic movements of the head, neck, eyes and trunk. Although SANDIFER initially observed the association, Kinsbourne and Oxon first reported it based on the observations of SANDIFER [1]. The syndrome is most certainly underrecognized, and delays in diagnosis are due to atypical presentations or cases in which the diagnosis is not part of the differential [2, 3].

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  • Cite

    APA: Copy

    NALBANTOGLU, BURCIN, METIN, DONMA M., & NALBANTOGLU, AYSIN. (2013). SANDIFER'S SYNDROME: A MISDIAGNOSED AND MYSTERIOUS DISORDER (LETTERS TO EDITOR). IRANIAN JOURNAL OF PEDIATRICS, 23(6), 715-716. SID. https://sid.ir/paper/660688/en

    Vancouver: Copy

    NALBANTOGLU BURCIN, METIN DONMA M., NALBANTOGLU AYSIN. SANDIFER'S SYNDROME: A MISDIAGNOSED AND MYSTERIOUS DISORDER (LETTERS TO EDITOR). IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2013;23(6):715-716. Available from: https://sid.ir/paper/660688/en

    IEEE: Copy

    BURCIN NALBANTOGLU, DONMA M. METIN, and AYSIN NALBANTOGLU, “SANDIFER'S SYNDROME: A MISDIAGNOSED AND MYSTERIOUS DISORDER (LETTERS TO EDITOR),” IRANIAN JOURNAL OF PEDIATRICS, vol. 23, no. 6, pp. 715–716, 2013, [Online]. Available: https://sid.ir/paper/660688/en

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