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

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Information Journal Paper

Title

TRIPLE X SYNDROME WITH SHORT STATURE: CASE REPORT AND LITERATURE REVIEW; CASE REPORT

Pages

  269-273

Abstract

 Background: TRIPLE X SYNDROME is a sex chromosomal aneuploidy condition characterized by tall stature, microcephaly, hypertelorism, congenital abnormalities, and motor and language delays. It is mainly derived from maternal nondisjunctional errors during meiosis. To highlight the clinical features and diagnosis of TRIPLE X SYNDROME, we present a rare phenotype of the syndrome.Case Presentation: A 5.9 year-old girl was admitted to our hospital because of SHORT STATURE. Both her height and weight were below the 3rd percentile compared to the normal peers. She was found with mild motor and speech delay. Laboratory investigation showed low level of IGF-1 and zinc, elevated estradiol level and normal result of arginine provocation test.Conclusion: Our data suggest that TRIPLE X SYNDROME should also be suspected in patients with SHORT STATURE, elevated estradiol and low level of IGF-1, even with normal result of arginine provocation test.

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    APA: Copy

    LI, MINGYAN, ZOU, CHAOCHUN, & ZHAO, ZHENGYAN. (2012). TRIPLE X SYNDROME WITH SHORT STATURE: CASE REPORT AND LITERATURE REVIEW; CASE REPORT. IRANIAN JOURNAL OF PEDIATRICS, 22(2), 269-273. SID. https://sid.ir/paper/628103/en

    Vancouver: Copy

    LI MINGYAN, ZOU CHAOCHUN, ZHAO ZHENGYAN. TRIPLE X SYNDROME WITH SHORT STATURE: CASE REPORT AND LITERATURE REVIEW; CASE REPORT. IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2012;22(2):269-273. Available from: https://sid.ir/paper/628103/en

    IEEE: Copy

    MINGYAN LI, CHAOCHUN ZOU, and ZHENGYAN ZHAO, “TRIPLE X SYNDROME WITH SHORT STATURE: CASE REPORT AND LITERATURE REVIEW; CASE REPORT,” IRANIAN JOURNAL OF PEDIATRICS, vol. 22, no. 2, pp. 269–273, 2012, [Online]. Available: https://sid.ir/paper/628103/en

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