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Cornelia de Lange Syndrome: Difference between revisions
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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== | ==Links== | ||
[File:Wikidata-logo-en.svg.png|32px] | |||
[https://www.wikidata.org/wiki/Q1133289 Q1133289] | |||
[http://www.ucdmc.ucdavis.edu/children/clinical_services/cleft_craniofacial/anomalies/cornelia.html Craniofacial anomalies – Cornelia de Lange Syndrome] | [http://www.ucdmc.ucdavis.edu/children/clinical_services/cleft_craniofacial/anomalies/cornelia.html Craniofacial anomalies – Cornelia de Lange Syndrome] | ||
Revision as of 13:25, 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]
Links
[File:Wikidata-logo-en.svg.png|32px] Q1133289