HETEROGENEITY OF SPONASTRIME DYSPLASIA - DELINEATION OF A VARIANT FORM WITH SEVERE MENTAL-RETARDATION

被引:1
|
作者
VERLOES, A
MISSON, JP
DUBRU, JM
JAMBLIN, P
LEMERRER, M
机构
[1] UNIV LIEGE,CHU SART TILMAN,CTR HUMAN GENET,B-4000 LIEGE,BELGIUM
[2] UNIV LIEGE,REG HOSP LA CITADELLE,DEPT RADIOL,LIEGE,BELGIUM
[3] UNIV LIEGE,REG HOSP LA CITADELLE,DEPT PAEDIAT,LIEGE,BELGIUM
[4] HOP NECKER ENFANTS MALAD,GENET MED CLIN,PARIS,FRANCE
[5] HOP NECKER ENFANTS MALAD,INSERM,U12,PARIS,FRANCE
关键词
SPONASTRIME SYNDROME; SHORT STATURE; OSTEOPENIA; METAPHYSEAL STRIATIONS; MENTAL RETARDATION;
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report a child with short stature, osteopenia with metaphyseal striations and severe mental retardation. This child shows radiological and clinical features of SPONASTRIME dysplasia. Only three sibships with this disorder have been reported. In two families, affected patients were of normal intelligence. In the third one, as well as our case, the dysplasia was complicated by severe mental retardation of unknown origin. The severity of the retardation in our case and a previous report, and some difference in the gestalt and radiological aspects, suggest that SPONASTRIME dysplasia is a heterogeneous disorder. We provisionally propose to split SPONASTRIME dysplasia in two phenotypically distinct subgroups, and to delineate here a 'new' variant with microcephaly and severe mental impairment.
引用
收藏
页码:208 / 215
页数:8
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