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Cornelia de Lange Syndrome: Difference between revisions
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disease||Cornelia de Lange Syndrome | {{disease|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.<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== | |||
{{wikidata|Q1133289}} | |||
[http://www.ucdmc.ucdavis.edu/children/clinical_services/cleft_craniofacial/anomalies/cornelia.html Craniofacial anomalies – Cornelia de Lange Syndrome] | |||
{{refs}} | |||
[[Category:Medicine]] | |||
[[nl:Cornelia de Lange]] | |||
Latest revision as of 01:24, 29 August 2023
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]
Links
Craniofacial anomalies – Cornelia de Lange Syndrome
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