Parental origin of mutations in sporadic cases of Treacher Collins syndrome

被引:30
|
作者
Splendore, A
Jabs, EW
Félix, TM
Passos-Bueno, MR
机构
[1] Univ Sao Paulo, Inst Biociencias, Dept Biol, Ctr Estudos Genoma Humano, Sao Paulo, Brazil
[2] Johns Hopkins Univ, Sch Med, Ctr Med Genet, Dept Pediat Med & Surg, Baltimore, MD 21205 USA
[3] Univ Fed Rio Grande Sul, Dept Genet, Hosp Clin Porto Alegre, Porto Alegre, RS, Brazil
关键词
Treacher Collins syndrome; TCOF1; parental age; sporadic mutation;
D O I
10.1038/sj.ejhg.5201029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In some autosomal dominant conditions, there is a correlation between new mutations and paternal age, with new mutations arising almost exclusively in the male germ line. To test this hypothesis in Treacher Collins syndrome, we analyzed 22 sporadic cases, determining the parental origin of the pathogenic mutation in 10 informative families. Mutations were found to be of both paternal and maternal origin, without a detectable parental age effect, confirming that a paternal age effect is not universal to all autosomal dominant disorders. A discussion on the parental origin of mutations and paternal age effect in other diseases is included.
引用
收藏
页码:718 / 722
页数:5
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