Wikisage, the free encyclopedia of the second generation, is digital heritage
Cornelia de Lange Syndrome: Difference between revisions
Jump to navigation
Jump to search
(Wikidata) |
m ([]) |
||
| Line 3: | Line 3: | ||
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] | [[File:Wikidata-logo-en.svg.png|32px]] | ||
[https://www.wikidata.org/wiki/Q1133289 Q1133289] | [https://www.wikidata.org/wiki/Q1133289 Q1133289] | ||
Revision as of 13:26, 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]
