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首页> 外文期刊>The Indian Journal of Pediatrics >Preliminary Report on Neonatal Screening for Congenital Hypothyroidism, Congenital Adrenal Hyperplasia and Glucose-6-Phosphate Dehydrogenase Deficiency: A Chandigarh Experience
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Preliminary Report on Neonatal Screening for Congenital Hypothyroidism, Congenital Adrenal Hyperplasia and Glucose-6-Phosphate Dehydrogenase Deficiency: A Chandigarh Experience

机译:新生儿筛查先天性甲状腺功能减退症,先天性肾上腺增生和葡萄糖6磷酸脱氢酶缺乏症的初步报告:Chandigarh的经验。

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摘要

To establish newborn screening in Indian scenario that could lay a framework for future such initiatives. Three disorders namely, congenital hypothyroidism (CH), congenital adrenal hyperplasia (CAH) and glucose-6-phosphate dehydrogenase deficiency (G-6-PDD) were selected for a preliminary study for newborn screening.
机译:在印度的情况下建立新生儿筛查,可以为将来的此类倡议奠定框架。先天性甲状腺功能减退(CH),先天性肾上腺皮质增生(CAH)和葡萄糖-6-磷酸脱氢酶缺乏症(G-6-PDD)三种疾病被选作新生儿筛查的初步研究。

著录项

  • 来源
    《The Indian Journal of Pediatrics》 |2010年第9期|969-973|共5页
  • 作者单位

    Genetic Centre Government Medical College ampamp Hospital Sector 32 Chandigarh India 160031;

    Genetic Centre Government Medical College ampamp Hospital Sector 32 Chandigarh India 160031;

    Department of Pediatrics Government Medical College ampamp Hospital Chandigarh India;

    Department of Pediatrics Government Medical College ampamp Hospital Chandigarh India;

    Genetic Centre Government Medical College ampamp Hospital Sector 32 Chandigarh India 160031;

    Genetic Centre Government Medical College ampamp Hospital Sector 32 Chandigarh India 160031;

    Genetic Centre Government Medical College ampamp Hospital Sector 32 Chandigarh India 160031;

    Genetic Centre Government Medical College ampamp Hospital Sector 32 Chandigarh India 160031;

    Department of Biochemistry Postgraduate Institute of Medical Education and Research Chandigarh India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Neonatal screening in India; Neonatal screening; Genetic disorders in India;

    机译:印度的新生儿筛查;新生儿的筛查;印度的遗传疾病;

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