Wikisage, the free encyclopedia of the second generation, is digital heritage
FGFR-Related Craniosynostosis Syndromes: Difference between revisions
Jump to navigation
Jump to search
m (todo) |
m (disease) |
||
Line 2: | Line 2: | ||
[[Kleeblattschädel syndrome]] (english cloverleaf skull) could appear | [[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> | ||
{{disease|craniosynostosis|Q75.0}} | |||
<references> | <references> |
Revision as of 23:21, 24 November 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]
Disease classification WHO
craniosynostosis Q75.0
<references>