FETAL AKINESIA-HYPOKINESIA SEQUENCE (PENA-SHOKEIR PHENOTYPE)

被引:7
|
作者
OBERLECHNER, E
SEIDEL, H
SCHRAMM, T
REHDER, H
GULLOTTA, F
STECHELE, F
HOGEL, B
ROTHEMUND, E
FICHTEL, G
机构
[1] AKAD LEHRKRK MUNCHEN HARLACHING,INST PATHOL,MUNICH,GERMANY
[2] UNIV MUNICH,KINDERPOLIKLIN,PADIATR GENET ABT,W-8000 MUNICH 2,GERMANY
[3] UNIV MUNICH,FRAUENKLIN 1,W-8000 MUNICH 2,GERMANY
[4] UNIV MARBURG,KLIN GENET ABT,W-3550 MARBURG,GERMANY
[5] UNIV MUNSTER,INST NEUROPATHOL,W-4400 MUNSTER,GERMANY
[6] AKAD LEHRKRK MUNCHEN NEUPEERLACU,INST PATHOL,MUNICH,GERMANY
[7] MAX PLANCK INST PSYCHIAT,NEUROPATHOL KLIN,W-8000 MUNICH 40,GERMANY
关键词
D O I
10.1055/s-2007-1022840
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The Pena Shokeir phenotype (PSP) is characterised by multiple ankyloses, camptodactyly, facial dysmorphisms and lung hypoplasia with hydramnios. The basic neuromuscular defect leads, through a fetal hypokinesia-akinesia, to the development of this non-specific phenotype and a respiratory insufficiency with early postnatal mortality. Severe central nervous anomalies are described in one-third of the reported cases. In this paper a foetus with PSP and 4 further foetuses with severe cerebral malformations and only discrete lung hypoplasia are described. It is not clear whether the cerebral malformations represent a primary or secondary developmental defect.
引用
收藏
页码:276 / 285
页数:10
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