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    •   صفحهٔ اصلی
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    • International Journal of Pediatrics
    • Volume 2, Issue 1
    • مشاهده مورد
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • International Journal of Pediatrics
    • Volume 2, Issue 1
    • مشاهده مورد
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    Glutaric Acidemia Type 1: Case Report

    (ندگان)پدیدآور
    Banikazemi, ZarinMazidi, MohsenNematy, Mohsen
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    اندازه فایل: 
    178.3کیلوبایت
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    زبان مدرک
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    نمایش کامل رکورد
    چکیده
    Introduction: Glutaric academia type I is a metabolic disorder that is caused due to deficiency of glutaryl-CoA dehydrogenase. Macrocephaly is a common sign in GA1, although many infants usually appear healthy at birth.   Case Report A 5.5 year old boy with GA1was admitted to NICU. Chief compliance of patient for hospitalization was pneumonia and sepsis and he was intubated and mechanically ventilated. This disease was diagnosed with signs of set developmental delay at 8 months oldand during these years; he was under control for nutritional counseling with a nutritionist and pediatrician. Nutritional support for this patient was in NICU.   Conclusion Medical treatment combined with nutritional support in GA1 managementsigns of serious illness; also dietary treatment control may are needed to reduce progression of the neurological damage.
    کلید واژگان
    Glutaric Academia
    Medical Treatment
    Neurological Damage

    شماره نشریه
    1
    تاریخ نشر
    2014-01-01
    1392-10-11
    ناشر
    Mashhad University of Medical Sciences
    سازمان پدید آورنده
    Biochemistry and Nutrition Research Center, Department of Nutrition, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
    Biochemistry and Nutrition Research Center, Department of Nutrition, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
    Biochemistry and Nutrition Research Center, Department of Nutrition, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

    شاپا
    2345-5047
    2345-5055
    URI
    https://dx.doi.org/10.22038/ijp.2014.2127
    http://ijp.mums.ac.ir/article_2127.html
    https://iranjournals.nlai.ir/handle/123456789/317434

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