Screening for the fragile X syndrome among mentally retarded males by hair root analysis

被引:0
作者
Tunçbilek, E [1 ]
Alikasifoglu, M
Aktas, D
Duman, F
Yanik, H
Anar, B
Oostra, B
Willemsen, R
机构
[1] Hacettepe Univ, Dept Pediat, Div Med Genet, TR-06100 Ankara, Turkey
[2] Erasmus Univ, Dept Clin Genet, CBG, NL-3000 DR Rotterdam, Netherlands
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2000年 / 95卷 / 02期
关键词
fragile X syndrome; FMRP; FMR1; screening; hair root analysis; prevalence;
D O I
10.1002/1096-8628(20001113)95:2<105::AID-AJMG3>3.0.CO;2-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A noninvasive antibody test was used to identify male fragile X patients in special education schools, on the basis of the lack of FMRP in hair roots. We studied 300 males with mental retardation of unknown cause attending special schools. Patients were divided into two groups, based on the scores according to a fragile X check list (Group 1 less than or equal to 9 points and Group 2 greater than or equal to 10 points). Group 2 consists of 51 males and only 5 males in this group showed no FMRP expression in hair roots within the abnormal range (91%), Fragile X diagnosis in these cases was confirmed by DNA analysis. None of the males scoring more than 10 on the check list was diagnosed positive for the fragile X syndrome using DNA analysis. With our antibody test on hair roots we did not detect a fragile X patient in Group 1, The FMRP antibody test on hair roots is suitable in a screening program for the fragile X syndrome among mentally retarded males attending special education schools. (C) 2000 Wiley-Liss.
引用
收藏
页码:105 / 107
页数:3
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