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FGFR-Related Craniosynostosis Syndromes: Difference between revisions
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FGFR-Related Craniosynostosis Syndromes comprises eight disorders comprising the FGFR-related craniosynostosis spectrum are Pfeiffer syndrome, Apert syndrome, Crouzon syndrome, Beare-Stevenson syndrome, FGFR2-related isolated coronal synostosis, Jackson-Weiss syndrome<ref>[https://www.ncbi.nlm.nih.gov/books/NBK1455/ GeneReview(R)]</ref> | FGFR-Related Craniosynostosis Syndromes comprises eight disorders comprising the FGFR-related craniosynostosis spectrum are Pfeiffer syndrome, Apert syndrome, Crouzon syndrome, Beare-Stevenson syndrome, FGFR2-related isolated coronal synostosis, Jackson-Weiss syndrome<ref>[https://www.ncbi.nlm.nih.gov/books/NBK1455/ GeneReview(R)]</ref> | ||
Kleeblattschädel syndrome (english | Kleeblattschädel syndrome (english cloverleaf skull) could appear | ||
<ref>https://www.ncbi.nlm.nih.gov/books/NBK5201/?report=reader</ref> | <ref>https://www.ncbi.nlm.nih.gov/books/NBK5201/?report=reader</ref> | ||
<references> | <references> | ||
Revision as of 15:12, 24 October 2015
FGFR-Related Craniosynostosis Syndromes comprises eight disorders comprising the FGFR-related craniosynostosis spectrum are Pfeiffer syndrome, Apert syndrome, Crouzon syndrome, Beare-Stevenson syndrome, FGFR2-related isolated coronal synostosis, Jackson-Weiss syndrome[1] Kleeblattschädel syndrome (english cloverleaf skull) could appear [2]
<references>