Wikisage, the free encyclopedia of the second generation, is digital heritage
Cornelia de Lange Syndrome: Difference between revisions
Jump to navigation
Jump to search
(Category:Medicine) |
m (nl+) |
||
| Line 2: | Line 2: | ||
Cornelia de Lange Syndrome (CdLS) is a very rare genetic disorder present from birth, but not always diagnosed at birth. It causes a range of physical, cognitive and medical challenges and affects both genders equally. The syndrome is named after Dutch pediatrician [[Cornelia de Lange|Cornelia Catharina de Lange]], who described it.<ref>https://en.wikipedia.org/w/index.php?title=Cornelia_de_Lange_Syndrome&oldid=677105911</ref> | Cornelia de Lange Syndrome (CdLS) is a very rare genetic disorder present from birth, but not always diagnosed at birth. It causes a range of physical, cognitive and medical challenges and affects both genders equally. The syndrome is named after Dutch pediatrician [[Cornelia de Lange|Cornelia Catharina de Lange]], who described it.<ref>https://en.wikipedia.org/w/index.php?title=Cornelia_de_Lange_Syndrome&oldid=677105911</ref> | ||
==Links== | |||
[http://www.ucdmc.ucdavis.edu/children/clinical_services/cleft_craniofacial/anomalies/cornelia.html Craniofacial anomalies – Cornelia de Lange Syndrome] | |||
<references/> | <references/> | ||
[[Category:Medicine]] | [[Category:Medicine]] | ||
[[nl:Cornelia de Lange]] | |||
Revision as of 13:22, 17 October 2015
Disease classification WHO
Q87.1 Cornelia de Lange Syndrome
Cornelia de Lange Syndrome (CdLS) is a very rare genetic disorder present from birth, but not always diagnosed at birth. It causes a range of physical, cognitive and medical challenges and affects both genders equally. The syndrome is named after Dutch pediatrician Cornelia Catharina de Lange, who described it.[1]