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Cornelia de Lange Syndrome: Difference between revisions
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{{disease|Q87.1|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><references/> | 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 Syndrome|Cornelia Catharina de Lange]], who described it.<ref>https://en.wikipedia.org/w/index.php?title=Cornelia_de_Lange_Syndrome&oldid=677105911</ref><references/> | ||
Revision as of 18:42, 8 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]