SUPPORT FOR THE NEWBORN SCREENING PILOT STUDIES RELATED ACTIVITIES

支持新生儿筛查试点研究相关活动

• 批准号: 10503157
• 负责人: WILLIAM WILCOX
• 金额: $ 0.25万
• 依托单位: EMORY UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-09-28 至 2022-09-27
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10503157
• 关键词: Advisory Committees; Affect; American; Cessation of life; Child; Child Health; Clinical; Collaborations; Contracts; Developmental Disabilities; Disease; Early Diagnosis; Early treatment; Evaluation; Goals; Hereditary Disease; Intellectual functioning disability; Left; Medical Genetics; Neonatal Screening; Nervous System Trauma; Newborn Infant; Pilot Projects; Rare Diseases; Recommendation; Reporting; Severities; medical schools; physically handicapped; screening guidelines; tool

The goal of newborn screening is to detect potentially fatal or disabling conditions in newborns, thereby providing a window of opportunity for early treatment, often while the child is still asymptomatic. Such early detection and treatment can have a profound impact on the clinical severity of the condition in the affected child. If left undiagnosed and untreated, the consequences of the targeted disorders can be dire, many causing irreversible neurological damage, intellectual, developmental, and physical disabilities, and even death. In 2006, the American College of Medical Genetics (ACMG) developed newborn screening guidelines that recommend that all newborn infants be screened for 29 "core conditions" and that 26 secondary conditions identified during the core evaluations be reported. These recommendations have been accepted by the HHS Secretary's Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC) (authorized by the Children's Health Act of 2000), and by the Secretary of HHS. Since acceptance of the core conditions, 5 additional ones have been added. Most states now use this or very similar panels for newborn screening. Currently, there are thousands of rare disorders that have been identified and hundreds that could potentially benefit from newborn screening.

新生儿筛查的目标是发现新生儿中可能致命或致残的疾病，从而为早期治疗提供机会，通常是在儿童仍无症状时。这种早期发现和治疗可以对受影响儿童的临床严重程度产生深远影响。如果不加以诊断和治疗，目标疾病的后果可能是可怕的，许多会造成不可逆转的神经损伤，智力，发育和身体残疾，甚至死亡。2006年，美国医学遗传学学会（ACMG）制定了新生儿筛查指南，建议对所有新生儿进行29种“核心疾病”的筛查，并报告在核心评估期间确定的26种次要疾病。这些建议已被卫生和公众服务部新生儿和儿童遗传性疾病秘书咨询委员会（ACHDNC）（经2000年《儿童健康法》授权）和卫生和公众服务部秘书接受。自接受核心条件以来，又添加了5个额外条件。大多数州现在使用这种或非常类似的面板进行新生儿筛查。目前，已经发现了数千种罕见疾病，数百种可能从新生儿筛查中受益。