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People with this syndrome experience a range of physical, cognitive, and medical challenges ranging from mild to severe. The syndrome has a widely varied phenotype, meaning people with the syndrome have varied features and challenges. Cornelia Catharina de Lange (24 June 1871 – 28 January 1950) was a Dutch pediatrician. Cornelia de Lange syndrome is named after her..

Cornelia de lange syndrome wikipedia

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Das Cornelia-de-Lange-Syndrom (CdLS) wird als Dysmorphiensyndrom bezeichnet, was multiple angeborene Fehlbildungen meint, die meist im Zusammenhang mit einer kognitiven Behinderung in Erscheinung treten. Cornelia de Lange, eine holländische Kinderärztin, beschrieb dieses Syndrom 1933. Cornelia de Lange Syndrome Cornelia De Lange Syndrome (CdLS) is a genetic condition which affects around 1 in every 10,000 live births. Individuals affected have the condition when born, but sometimes it is not diagnosed until later.

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It is referred to as a syndrome because there is a range of features and characteristics associated with it; individuals with CdLS may have only a few or all of the symptoms. Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Cornelia de Lange syndrome. The TRIP database provides clinical publications about evidence-based medicine.

Cornelia de lange syndrome wikipedia

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Synonyms . Amsterdam dwarfism; References .

Cornelia de lange syndrome wikipedia

Life. Born in Alkmaar, De Lange graduated from the University of Amsterdam in 1897 and began her general practice.
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Management of Genetic Syndromes, Cornelia de Lange syndrome (chapter 15), kustantaja Wiley, 3.
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Robbins, Arnold, Beebe, Nelson HF Classic Shell Scripting

It is caused by variants in any one of seven genes, all of which ha … Cornelia de Lange syndrome (CdLS; MIM #122470, 300590, 610759, 614701, 300882) is a rare and clinically variable disorder that affects multiple organs. It is characterized by intellectual disability (mild to severe), distinctive facial features, prenatal and postnatal growth retardation, and hirsutism.