Structured Summary
Abstract
A chromosomal disorder characterized by MENTAL RETARDATION, broad thumbs, webbing of fingers and toes, beaked nose, short upper lip, pouting lower lip, agenesis of corpus callosum, large foramen magnum, keloid formation, pulmonary stenosis, vertebral anomalies, chest wall anomalies, sleep apnea, and megacolon. The disease has an autosomal dominant pattern of inheritance and is associated with deletions of the short arm of chromosome 16 (16p13.3).
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Classification
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Synonyms
10 entry terms
- Broad Thumb-Hallux Syndrome
- Broad Thumbs and Great Toes, Characteristic Facies, and Mental Retardation
- Rubinstein Syndrome
- Broad Thumb Hallux Syndrome
- Broad Thumb-Hallux Syndromes
- Rubinstein Taybi Syndrome
- Syndrome, Broad Thumb-Hallux
- Syndrome, Rubinstein
- Syndrome, Rubinstein-Taybi
- Syndromes, Broad Thumb-Hallux
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
91(72); was see under ABNORMALITIES, MULTIPLE 1972-90
MeSH Record
Previous Indexing
- Abnormalities, Multiple (1968-1971)
- Mental Retardation (1966-1971)
MeSH Hierarchy
Tree Numbers
MeSH Record
NLM Classification
QS 675
AMA Style
References
- National Library of Medicine. Rubinstein-Taybi Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D012415. http://id.nlm.nih.gov/mesh/2026/D012415
- Rubinstein-Taybi Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Rubinstein%E2%80%93Taybi_syndrome
- Rubinstein-Taybi Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q666980