PARTIAL DELETION OF THE LONG ARM OF CHROMOSOME-11 [DEL(11)(Q23.3-]QTER)] WITH ABNORMAL WHITE MATTER

被引:35
作者
WARDINSKY, TD
WEINBERGER, E
PAGON, RA
CLARREN, SK
THULINE, HC
机构
[1] UNIV WASHINGTON,CHILDRENS HOSP & MED CTR,DEPT PEDIAT,DIV CONGENIT DEFECTS,SEATTLE,WA 98105
[2] UNIV WASHINGTON,CHILDRENS HOSP & MED CTR,DEPT PEDIAT,DIV MED GENET,SEATTLE,WA 98105
[3] UNIV WASHINGTON,CHILDRENS HOSP & MED CTR,DEPT PEDIAT,DIV RADIOL,SEATTLE,WA 98105
[4] WASHINGTON STATE CYTOGENET LAB,SEATTLE,WA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1990年 / 35卷 / 01期
关键词
Chromosome; 11; deletion; mca/mr syndrome; Myelin abnormality; Trigonocephaly;
D O I
10.1002/ajmg.1320350111
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A patient with partial deletion of the long arm of chromosome 11[del(11)(q23.3→qter)] had macrocephalic trigonocephaly, growth and mental retardation, congenital heart defect, and characteristic facial appearance familiar to that of 33 other reported patients with this deletion. Computed tomography (CT) and magnetic resonance imaging of this infant's brain demonstrated abnormality of the supratentorial white matter. This may represent either deficiency or delay in myelination or possibly a demyelination process. No abnormalities in white matter were described in seven of 33 previously reported patients whose brains were examined by ultrasound, CT, or autopsy.
引用
收藏
页码:60 / 63
页数:4
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