Document Detail


Three siblings with Walker-Warburg Syndrome.
MedLine Citation:
PMID:  8780938     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The Walker-Warburg syndrome (WWS) is an autosomal recessive disease entity within the framework of "cerebro-ocular-muscular syndromes". The gene locus is still undetected. Its diagnostic criteria have been firmly established in the literature on newborns or infants affected with the disease. However, a diagnosis of severe pathologic conditions must often be made on the basis of ultrasound examination at a fetal age. It is therefore necessary to examined whether the diagnostic criteria are sufficient to warrant a diagnosis at the fetal stage. We here report on a new family affected with WWS. Two elder siblings had presented with epileptic seizures, eye abnormalities as well as multiple skeletal dysplasias (the latter finding in the first child only) in the neonatal period, and died in their first years. Postmortem examination of the second child revealed type II lissencephaly, buphthalmos, and undifferentiated retina with rigid retinal folds. Skeletal muscle tissue was not examined. In a sibling fetus, bilateral cataract was detected in the 17th gestational week by ultrasonographic examination. Postmortem examination in the 23rd gestational week revealed type II lissencephaly and bilateral cataract. Skeletal muscle was normal. Taken together, all siblings were diagnosed as Walker-Warburg syndrome. In the fetal case, prenatal diagnosis could only be made with confidence against a background of a positive family history.
Authors:
A Bornemann; R Pfeiffer; E Beinder; H Wenkel; U Schlicker; R Meyermann; T Kirchner
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  General & diagnostic pathology     Volume:  141     ISSN:  0947-823X     ISO Abbreviation:  Gen Diagn Pathol     Publication Date:  1996 May 
Date Detail:
Created Date:  1997-01-21     Completed Date:  1997-01-21     Revised Date:  2005-11-17    
Medline Journal Info:
Nlm Unique ID:  9511700     Medline TA:  Gen Diagn Pathol     Country:  GERMANY    
Other Details:
Languages:  eng     Pagination:  371-5     Citation Subset:  IM    
Affiliation:
Department of Pathology, University of Erlangen, Germany.
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple / pathology*
Abortion, Induced
Brain / abnormalities*
Eye Abnormalities / pathology*
Female
Humans
Hydrocephalus / pathology
Infant, Newborn
Male
Muscular Dystrophies / pathology*
Nuclear Family
Obstetric Labor, Premature
Pregnancy
Retinal Dysplasia / pathology
Syndrome

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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