De Lange Syndrome

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"De Lange Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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)

Descriptor ID	D003635
MeSH Number(s)	C10.597.606.643.210 C16.131.077.272 C16.131.260.210 C16.320.180.210
Concept/Terms	De Lange Syndrome De Lange Syndrome Syndrome, De Lange Cornelia De Lange Syndrome Brachmann-De Lange Syndrome Brachmann De Lange Syndrome Syndrome, Brachmann-De Lange De Lange's Syndrome Syndrome, De Lange's Typus Degenerativus Amstelodamensis Amstelodamensis, Typus Degenerativus Cornelia de Lange Syndrome 2 Cornelia de Lange Syndrome 2 Cornelia de Lange Syndrome, X-Linked Cornelia de Lange Syndrome, X Linked Cornelia de Lange Syndrome 3 Cornelia de Lange Syndrome 3 Cornelia de Lange Syndrome 1 Cornelia de Lange Syndrome 1

Below are MeSH descriptors whose meaning is more general than "De Lange Syndrome".

Diseases [C]
Nervous System Diseases [C10]
Neurologic Manifestations [C10.597]
Neurobehavioral Manifestations [C10.597.606]
Intellectual Disability [C10.597.606.643]
De Lange Syndrome [C10.597.606.643.210]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
De Lange Syndrome [C16.131.077.272]
Chromosome Disorders [C16.131.260]
De Lange Syndrome [C16.131.260.210]
Genetic Diseases, Inborn [C16.320]
Chromosome Disorders [C16.320.180]
De Lange Syndrome [C16.320.180.210]

Below are MeSH descriptors whose meaning is related to "De Lange Syndrome".

Below are MeSH descriptors whose meaning is more specific than "De Lange Syndrome".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "De Lange Syndrome" by people in UAMS Profiles by year, and whether "De Lange Syndrome" was a major or minor topic of these publications.

Bar chart showing 1 publications over 1 distinct years, with a maximum of 1 publications in 2020

To see the data from this visualization as text, click here.

People

Gonzalez Garcia, Aixa

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Similar Concepts

Top Journals

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