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) |
No edit summary |
||
(2 intermediate revisions by the same user not shown) | |||
Line 3: | Line 3: | ||
<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}} | |||
{{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: |