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21-Hydroxylase Deficiency: Newborn Screening in Iran?
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نویسنده
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Mahdieh Nejat ,Rabbani Bahareh ,Rabbani Ali
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منبع
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innovative journal of pediatrics - 2012 - دوره : 22 - شماره : 3 - صفحه:279 -280
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چکیده
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21-hydroxylase deficiency (21-ohd) accounts for the cause of 90-95% of congenital adrenal hyperplasia (cah) cases. the world incidence of 21-ohd is 1:20,000 to 1:10,000 live births[1]. prevalence of cah trends to be high due to frequent consanguineous and first cousin marriages and underestimation because of stigmatization[2,3].
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کلیدواژه
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21-hydroxylase Deficiency; Congenital Adrenal Hyperplasia; Screening
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آدرس
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TehranUniversity of Medical Sciences, Growth and Development Research Center, ایران. ilam university of medical sciences, Faculty of Medicine, ایران, tehran university of medical sciences tums, Growth and Development Research Center, ایران, tehran university of medical sciences tums, Growth and Development Research Center, Pediatrics Center of Excellence, ایران
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پست الکترونیکی
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rabania@tums.ac.ir
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Authors
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