Maternal isochromosome 7q and paternal isochromosome 7p in a boy with growth retardation

被引:8
作者
Kotzot, D
Holland, H
Keller, E
Froster, UG
机构
[1] Univ Leipzig, Inst Humangenet, D-04103 Leipzig, Germany
[2] Univ Leipzig, Childrens Hosp, D-7010 Leipzig, Germany
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2001年 / 102卷 / 02期
关键词
isochromosome; 7p; 7q; Silver-Russell syndrome; UPD; 7;
D O I
10.1002/ajmg.1430
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A 12-year 9-month-old boy with postnatal growth retardation, normal psychomotor development, and minor anomalies that included a triangular-shaped face, small nose, and narrow and high-arched palate is reported. The constitutional karyotype was 46,XY,i(7)(p10),i(7)(q10). Molecular investigations revealed the presence of a maternal isodisomy 7q and a paternal isodisomy 7p. The clinical and molecular findings are notably congruent with a recently reported case and support the hypothesis of one or more maternally imprinted genes located on the long arm of chromosomes 7 that regulate, in particular, postnatal growth. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:169 / 172
页数:4
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