Methylenetetrahydrofolate reductase deficiency in a patient with phenotypic findings of Angelman syndrome

被引:0
|
作者
Arn, PH
Williams, CA
Zori, RT
Driscoll, DJ
Rosenblatt, DS
机构
[1] Nemours Childrens Clin, Div Genet, Dept Pediat, Jacksonville, FL 32207 USA
[2] RC Philips, Res Unit, Gainesville, FL USA
[3] McGill Univ, Dept Med, Div Med Genet, Montreal, PQ, Canada
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1998年 / 77卷 / 03期
关键词
methylenetetrahydrofolate reductase deficiency; methylenetetrahydrofolate reductase; Angelman syndrome;
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Deficiency of methylenetetrahydrofolate. reductase (MTHFR) is associated with a variable phenotype that includes mental retardation, gait abnormalities, and seizures. Many of the same clinical findings are also seen in patients with Angelman syndrome. We report on a patient with MTHFR deficiency who was initially diagnosed as having Angelman syndrome. This case illustrates that MTHFR deficiency can mimic the phenotype of Angelman syndrome and that MTHFR deficiency should be excluded in patients with manifestations of Angelman syndrome whose molecular studies of chromosome 15 are normal. (C) 1998 Wiley-Liss, Inc.
引用
收藏
页码:198 / 200
页数:3
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