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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 trefoil skull) could appears
[[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>
{{disease|craniosynostosis|Q75.0}}
 
{{refs}}
 
[[Category:Disease]]

Latest revision as of 02:29, 11 May 2019

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]

Disease classification WHO
craniosynostosis Q75.0

References

References: