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GENETICS AND DEAFNESS: IMPLICATIONS FOR EDUCATION AND LIFE CARE OF DEAF STUDENTS

机译:遗传与聋哑:对聋哑学生的教育和生活护理的意义

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摘要

THE SEVERITY of deafness can obscure the presence of other disabilities that may accompany genetic anomalies, such as occur in Alport and Usher syndromes. Recent advances in genetics have heightened attention to various disabilities and dysfunctions that may coexist with deafness. Failure to recognize these additional disabilities when they occur can misguide educational planning; may open the afflicted deaf person to failure to identify, diagnose, and manage potentially serious health conditions; and in some instances may even lead to loss of life. Of the many genetic conditions that have been identified, a few examples are cited to illustrate the need to inform parents, educators, and other caregivers about the importance of obtaining genetic information. [PUBLICATION ABSTRACT]
机译:耳聋的严重程度可以掩盖可能伴随遗传异常的其他残疾,例如Alport和Usher综合征。遗传学的最新进展已引起人们对可能与耳聋并存的各种残疾和功能障碍的关注。如果无法及时识别出这些额外的残疾,可能会误导教育计划;可能使患病的聋人无法识别,诊断和管理潜在的严重健康状况;在某些情况下甚至可能导致生命损失。在已经确定的许多遗传状况中,列举了一些例子来说明有必要告知父母,教育者和其他看护人有关获取遗传信息的重要性。 [出版物摘要]

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  • 来源
    《American Annals of the Deaf》 |2008年第4期|p.408-410|共3页
  • 作者单位

    JEROME D. SCHEIN AND MAURICE H. MILLERSCHEIN AND MILLER ARE EMERITUS PROFESSORS, STEINHARDT SCHOOL OF CULTURE, EDUCATION, AND HUMAN DEVELOPMENT, NEW YORK UNIVERSITY.;

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