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Common primary fibroblastic growth factor receptor-related craniosynostosis syndromes: A pictorial review.
MedLine Citation:
PMID:  21042516     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
Mutations in different types of fibroblastic growth factor receptors (FGFRs) have been associated with a variety of phenotype abnormalities, the common ones being Apert, Crouzon and Pfeiffer syndromes. In this study, we present two representative cases having the Apert and Pfeiffer syndromes, respectively, and discuss their clinical presentation, sequel and surgical implications.
Authors:
Rohit K Singh; Jitendra Singh Verma; Arun K Srivastava; Awadhesh K Jaiswal; Sanjay Behari
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Journal of pediatric neurosciences     Volume:  5     ISSN:  1998-3948     ISO Abbreviation:  J Pediatr Neurosci     Publication Date:  2010 Jan 
Date Detail:
Created Date:  2010-11-02     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101273794     Medline TA:  J Pediatr Neurosci     Country:  India    
Other Details:
Languages:  eng     Pagination:  72-5     Citation Subset:  -    
Affiliation:
Department of Neurosurgery, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
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