| Common primary fibroblastic growth factor receptor-related craniosynostosis syndromes: A pictorial review. | |
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MedLine Citation:
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PMID: 21042516 Owner: NLM Status: In-Data-Review |
Abstract/OtherAbstract:
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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. |
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Authors:
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Rohit K Singh; Jitendra Singh Verma; Arun K Srivastava; Awadhesh K Jaiswal; Sanjay Behari |
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Publication Detail:
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Type: Journal Article |
Journal Detail:
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Title: Journal of pediatric neurosciences Volume: 5 ISSN: 1998-3948 ISO Abbreviation: J Pediatr Neurosci Publication Date: 2010 Jan |
Date Detail:
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Created Date: 2010-11-02 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 101273794 Medline TA: J Pediatr Neurosci Country: India |
Other Details:
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Languages: eng Pagination: 72-5 Citation Subset: - |
Affiliation:
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Department of Neurosurgery, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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