Description. Cornelia de Lange syndrome is a developmental disorder that affects many parts of the body. The features of this disorder vary widely among affected individuals and range from relatively mild to severe. Cornelia de Lange syndrome is characterized by slow growth before and after birth leading to short stature; intellectual.. Cornelia de Lange syndrome (CdLS) was described, in 1933, by the Dutch pediatrician, Cornelia Catharina de Lange, who illustrated two unrelated girls with similar features.[1] Previously, in 1849, the anatomist Willem Vrolik (1801-1863) reported a case as an extreme example of oligodactyly, and the German doctor Brachmann published, in 1916, a case of symmetric monodactyly, antecubital.

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Cornelia De Lange Syndrome What Is Cornelia de Lange Syndrome?

Cornelia de Lange syndrome causes, symptoms, prognosis and treatment

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Syndrome de Cornelia de Lange Symptômes, causes, diagnostic et traitement

Cornelia de Lange syndrome (CdLS) (Online Mendelian Inheritance in Man (OMIM) entries 122470, 300590, 300882, 610759 and 614701) is a multisystem disorder with physical, cognitive and behavioural.. Cornelia de Lange syndrome (CdLS) is a rare genetic condition that affects growth and development and can range from mild to severe. A child's growth before and after birth is often slower, and they may have short stature. Children with this condition may also have moderate to severe intellectual disability, behavior problems, and autism.People with CdLS often have distinct facial features.