Williams Charles A, Beaudet Arthur L, Clayton-Smith Jill, Knoll Joan H, Kyllerman Martin, Laan Laura A, Magenis R Ellen, Moncla Ann, Schinzel Albert A, Summers Jane A, Wagstaff Joseph
Department of Pediatrics, Division of Genetics, R.C. Philips Unit, University of Florida, Gainesville, Florida 32610, USA.
Am J Med Genet A. 2006 Mar 1;140(5):413-8. doi: 10.1002/ajmg.a.31074.
In 1995, a consensus statement was published for the purpose of summarizing the salient clinical features of Angelman syndrome (AS) to assist the clinician in making a timely and accurate diagnosis. Considering the scientific advances made in the last 10 years, it is necessary now to review the validity of the original consensus criteria. As in the original consensus project, the methodology used for this review was to convene a group of scientists and clinicians, with experience in AS, to develop a concise consensus statement, supported by scientific publications where appropriate. It is hoped that this revised consensus document will facilitate further clinical study of individuals with proven AS, and assist in the evaluation of those who appear to have clinical features of AS but have normal laboratory diagnostic testing.
1995年,为总结天使综合征(AS)的显著临床特征以帮助临床医生及时准确诊断,发表了一份共识声明。鉴于过去十年取得的科学进展,现在有必要重新审视原始共识标准的有效性。与原始共识项目一样,本次综述采用的方法是召集一组在AS方面有经验的科学家和临床医生,制定一份简洁的共识声明,并在适当情况下得到科学出版物的支持。希望这份修订后的共识文件将有助于对已确诊AS的个体进行进一步的临床研究,并协助评估那些看似具有AS临床特征但实验室诊断测试正常的患者。