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

مقاله طرح

مشخصات مقاله

مجری: واحد استان فارس
سال:1386 | تاریخ پایان: اسفند 1386

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

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

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

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

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

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اطلاعات طرح

عنوان

Congenital Hypothyroidism as the main cause of G6PD deficiency phenotype in neonates

نهاد حامی(کارفرما)

 جهاد دانشگاهی

نویسندگان

سارا-سنمار

صفحات

 صفحه شروع | صفحه پایان

کلیدواژه

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چکیده

 Glucose-6-phosphate dehydrogenates (G6PD) deficiency is the most common defects of red blood cells among Iranian and Mediterranean people. Hypothyroidism is defined as thyroid hormone deficiency starting from the time of birth. Thyroid hormones influence the activity of lipogenic enzymes such as glucose-6-phosphate dehydrogenase and malic enzyme. This study aimed to determine the rate of hypothyroidism in patients with G6PD deficiency. After 120 days, the newborns that administered drug and diet for hypothyroidism were checked for TSH and G6PD enzyme. 2287 out of 23260 screened babies were afflicted with favism (512 females and 1775 males). 42 cases were hypothyroid among who 35 had G6PD deficiency. However, after 120 days of treatment with Levothyroxine, 23(85%) patients of them had normal levels of G6PD.It shows that their deficiency had no genetic origin. Base on these findings of this study, the newborns with G6PD deficiency should be checked for thyroid hormones. Moreover, in the hypothyroid patients, checking the level of G6PD is recommended.

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    APA: کپی

    سنمار، سارا. (اسفند 1386). Congenital Hypothyroidism as the main cause of G6PD deficiency phenotype in neonates. تهران، ایران: مراکز جهاد دانشگاهی. https://sid.ir/paper/790221/fa

    Vancouver: کپی

    سنمار سارا. [Internet]. Congenital Hypothyroidism as the main cause of G6PD deficiency phenotype in neonates. تهران، ایران: مراکز جهاد دانشگاهی؛ اسفند 1386. Available from: https://sid.ir/paper/790221/fa

    IEEE: کپی

    سارا سنمار، “Congenital Hypothyroidism as the main cause of G6PD deficiency phenotype in neonates،” ایران، مراکز جهاد دانشگاهی، اسفند 1386. [Online]. Available: https://sid.ir/paper/790221/fa

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