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Information Journal Paper

Title

FREQUENCY OF GENETIC DISORDERS IN HOSPITALIZED CHILDREN IN PEDIATRIC WARD

Pages

  25-31

Abstract

 Genetic problems have known as important causes of pediatric diseases. Recent research in the world shows that nearly half of the children hospitalized in PEDIATRIC WARD have GENETIC DISORDERS. There is no such record in Iran. Present study is a descriptive case-series, which evaluate the frequency of GENETIC DISORDERS in PEDIATRIC WARD and the duration of their stay in hospital for the first time in Iran. Four hundred and ninety nine children admitted in PEDIATRIC WARD were evaluated. A questioner was filed for each child, which were included age, sex, final diagnosis and duration of stay in bed. This study was done in PEDIATRIC WARD of Yazd Shahid Sadoughi Hospital. From 499 children 13.8% suffer from SINGLE GENE and CHROMOSOMAL DISORDERS, 40.8% MULTIFACTORIAL, 35.8% non GENETIC DISORDERS and 9.6% unknown cases. Duration of stay in hospital with and without GENETIC DISORDERS was not significantly different. In conclusion, genetic diseases all together are not rare and nearly half of the children admitted to PEDIATRIC WARD hospitalized because of them. So genetic counseling in children is very important evaluation for prevention of GENETIC DISORDERS.

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  • Cite

    APA: Copy

    GHASEMI, N., SADR BAFGHI, S.M., & SHAMS, H.. (2011). FREQUENCY OF GENETIC DISORDERS IN HOSPITALIZED CHILDREN IN PEDIATRIC WARD. MODERN GENETICS JOURNAL (MGJ), 6(3 (26)), 25-31. SID. https://sid.ir/paper/116632/en

    Vancouver: Copy

    GHASEMI N., SADR BAFGHI S.M., SHAMS H.. FREQUENCY OF GENETIC DISORDERS IN HOSPITALIZED CHILDREN IN PEDIATRIC WARD. MODERN GENETICS JOURNAL (MGJ)[Internet]. 2011;6(3 (26)):25-31. Available from: https://sid.ir/paper/116632/en

    IEEE: Copy

    N. GHASEMI, S.M. SADR BAFGHI, and H. SHAMS, “FREQUENCY OF GENETIC DISORDERS IN HOSPITALIZED CHILDREN IN PEDIATRIC WARD,” MODERN GENETICS JOURNAL (MGJ), vol. 6, no. 3 (26), pp. 25–31, 2011, [Online]. Available: https://sid.ir/paper/116632/en

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