Literature DB >> 8050688

[Familial akinesia-hypokinesia sequence (Pena-Shokier phenotype)].

E Oberlechner1, H Seidel, T Schramm, H Rehder, F Gullotta, F Stechele, B Högel, E Rothemund, G Fichtel.   

Abstract

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 nonspecific 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.

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Year:  1994        PMID: 8050688     DOI: 10.1055/s-2007-1022840

Source DB:  PubMed          Journal:  Geburtshilfe Frauenheilkd        ISSN: 0016-5751            Impact factor:   2.915


  1 in total

1.  Progressive Respiratory Insufficiency in a Teenager with Diaphragmatic Hypomotility Due to a Novel Combination of Gliomedin Gene Variants.

Authors:  Benjamin Eurich; Catharina Nitsche; Margot Lau; Britta Hanker; Juliane Spiegler; Guido Stichtenoth
Journal:  Children (Basel)       Date:  2022-05-28
  1 in total

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