Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Chromosome Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
...
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Preferred term
De Lange Syndrome
Type
-
Topical Descriptor
Broader concept
Entry terms
- Amstelodamensis, Typus Degenerativus
- Brachmann De Lange Syndrome
- Brachmann-De Lange Syndrome
- Cornelia De Lange Syndrome
- De Lange's Syndrome
- Syndrome, Brachmann-De Lange
- Typus Degenerativus Amstelodamensis
Scope note
- A syndrome characterized by growth retardation, severe MENTAL RETARDATION, short stature, a low-pitched growling cry, brachycephaly, low-set ears, webbed neck, carp mouth, depressed nasal bridge, bushy eyebrows meeting at the midline, hirsutism, and malformations of the hands. The condition may occur sporadically or be associated with an autosomal dominant pattern of inheritance or duplication of the long arm of chromosome 3. (Menkes, Textbook of Child Neurology, 5th ed, p231)
History note
- 2000(1964)
In other languages
-
Finnish
-
Cornelia de Lange
-
Cornelia de Langen syndrooma
-
de Lange
-
De Langen oireyhtymä
-
de Langen syndrooma
-
syndroma de Lange
-
Swedish
-
Brachmann-de Langes syndrom
-
Cornelia de Langes syndrom
URI
http://www.yso.fi/onto/mesh/D003635
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