AN UNUSUAL TYPE OF ACROCEPHALOSYNDACTYLY WITH BILATERAL PARIETOOCCIPITAL ENCEPHALOCELE, MICROPENIS, AND SEVERE MENTAL-RETARDATION

被引：15

作者：

LORENZ, P ^{[1
]}

RUPPRECHT, E ^{[1
]}

TELLKAMP, H ^{[1
]}

机构：

[1] MED ACAD CARL GUSTAV CARUS,DEPT RADIOL,O-8019 DRESDEN,GERMANY

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1990年 / 36卷 / 03期

关键词：

craniostenosis; syndactyly;

D O I：

10.1002/ajmg.1320360302

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Here we report on a 2 year 3-month-old boy with acrocephalosyndactyly, a bilateral parietooccipital 'encephalocele,' micropenis, and severe mental retardation. To our knowledge there are no other reports of similarly affected patients in the literature

引用

页码：265 / 268

页数：4

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