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首页> 外文期刊>American journal of medical genetics, Part A >A tribute to our teacher, Dr. Judith Hall: a child with the trait of the Earl of Shrewsbury.
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A tribute to our teacher, Dr. Judith Hall: a child with the trait of the Earl of Shrewsbury.

机译:向我们的老师朱迪思·霍尔博士致敬:这个孩子具有什鲁斯伯里伯爵的特征。

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摘要

"Organized human endeavor can be lifted an order of magnitude through teaching if it is inspiring" (Editor, Am J Dis Child, 1972). The benevolent influence of Dr. Judy Hall's inspiring clinical teaching in the field of genetic syndromes and birth defects is illustrated through the eventual surgical remediation of conductive hearing loss for a 4-year-old girl with unusual knuckles. The fascinating history of this child's syndrome has been further explored in the descendents of the first Earl of Shrewsbury. The legends of his story and his role in the Hundred Years War were immortalized by William Shakespeare in his play Henry VI Part I, but neither Shakespeare nor historians documented that the Earl actually had abnormal finger joints. Heterozygous mutations in the human noggin gene (NOG) cause a spectrum of joint fusions, including this child's traits. On behalf of practitioners of medicine, pediatrics, clinical genetics, and dysmorphology, as well as research scientists in the many domains of genetics, thank you, Judy, for your inspiration, enthusiasm, and teaching.
机译:“如果有启发性,可以通过教学将有组织的人类努力提升一个数量级”(编辑,Am J Dis Child,1972年)。朱迪·霍尔(Judy Hall)博士在遗传综合症和先天缺陷领域的启发性临床教学的有益影响,通过最终手术矫正了一名四肢不正常指关节的4岁女孩的传导性听力损失而得到了说明。在什鲁斯伯里伯爵的第一个伯爵的后代中,进一步探索了这个孩子的综合症的迷人历史。威廉·莎士比亚(William Shakespeare)在其戏剧《亨利六世》(Henry VI Part I)中使他的故事传奇和他在百年战争中的角色不朽,但莎士比亚和历史学家都没有记载伯爵实际上有异常的指关节。人头蛋白基因(NOG)中的杂合突变会导致一系列关节融合,包括这个孩子的性状。我代表医学,儿科,临床遗传学和畸形学的执业医师以及遗传学许多领域的研究科学家,感谢朱迪,感谢您的启发,热情和教学。

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