Document Detail


Klippel-Feil syndrome revisited: diagnostic pitfalls impacting neurosurgical management.
MedLine Citation:
PMID:  1394279     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Klippel-Feil syndrome in its most basic definition includes several anomalous conditions of the cervicomedullary junction and suboccipital region. Pediatric neurosurgeons are often involved in surgical palliation of this syndrome, without realizing how the accompanying anomalies may obfuscate management in the older child. A brief review of the embryology of the rhombencephalon helps to clarify the etiology of some of these symptoms which may cause confusion and, occasionally, inappropriate treatment. Illustrative cases will demonstrate some of these pitfalls. Appropriate early intervention, such as posterior fossa decompression, ventricular shunting, and fundal plication, may help to avoid needless morbidity. The advent of magnetic resonance scanning has helped to clarify the diagnosis and resulted in more appropriate treatment in these cases.
Authors:
M C Johnson
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery     Volume:  8     ISSN:  0256-7040     ISO Abbreviation:  Childs Nerv Syst     Publication Date:  1992 Sep 
Date Detail:
Created Date:  1992-11-23     Completed Date:  1992-11-23     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  8503227     Medline TA:  Childs Nerv Syst     Country:  GERMANY    
Other Details:
Languages:  eng     Pagination:  322-5     Citation Subset:  IM    
Affiliation:
Division of Pediatric Neurosurgery, Children's Health Care Center, Emanuel Hospital, Portland, OR 97227.
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MeSH Terms
Descriptor/Qualifier:
Female
Humans
Infant, Newborn
Klippel-Feil Syndrome / diagnosis*,  surgery*
Magnetic Resonance Imaging
Male
Neurosurgery
Postoperative Complications

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


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