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Information Journal Paper

Title

DELAYED DIAGNOSIS OF TURNER'S SYNDROME: A PROBLEM IN TREATMENT OF SHORT STATURE

Author(s)

VAKILI R. | Issue Writer Certificate 

Pages

  203-208

Abstract

 Average age at diagnosis, clinical features, and karyotype analysis of 40 girls with TURNER'S SYNDROME (TS) were studied. The medical records of 40 girls with TS were reviewed for age at diagnosis, clinical features, karyotype analysis and reasons of admission in pediatric endocrinology ward. Although lymphedema is the key to diagnosis in newborn period, none of the cases were diagnosed in infancy. The average age at diagnosis was 13.4 years. All of the cases admitted for evaluation of SHORT STATURE, and 14 of them had delayed puberty too. 50 percent of the patients had a chromosomal constitution 45X, 22.5% were mosaic, 15% isochromosom and the remaining 12.5% had other karyotypes. The diagnosis of TS is often delayed, and this deranged the appropriate treatment of SHORT STATURE. We recommend cytogenetic analysis of all girls with lymphedema, unexplained SHORT STATURE, webbed neck, short neck, low posterior hairline and multiple nevi.

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    APA: Copy

    VAKILI, R.. (2002). DELAYED DIAGNOSIS OF TURNER'S SYNDROME: A PROBLEM IN TREATMENT OF SHORT STATURE. JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES, 9(4), 203-208. SID. https://sid.ir/paper/211/en

    Vancouver: Copy

    VAKILI R.. DELAYED DIAGNOSIS OF TURNER'S SYNDROME: A PROBLEM IN TREATMENT OF SHORT STATURE. JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2002;9(4):203-208. Available from: https://sid.ir/paper/211/en

    IEEE: Copy

    R. VAKILI, “DELAYED DIAGNOSIS OF TURNER'S SYNDROME: A PROBLEM IN TREATMENT OF SHORT STATURE,” JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES, vol. 9, no. 4, pp. 203–208, 2002, [Online]. Available: https://sid.ir/paper/211/en

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