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Cornelia de Lange Syndrome: Difference between revisions
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[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] | ||
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[[Category:Medicine]] | [[Category:Medicine]] | ||
[[nl:Cornelia de Lange]] | [[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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