"Rubinstein-Taybi 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.
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).
Descriptor ID |
D012415
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MeSH Number(s) |
C05.116.099.370.797 C05.660.207.850 C10.597.606.643.700 C16.131.077.804 C16.131.260.790 C16.131.621.207.850 C16.320.180.790
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Concept/Terms |
Rubinstein-Taybi Syndrome- Rubinstein-Taybi Syndrome
- Rubinstein Taybi Syndrome
- Syndrome, Rubinstein-Taybi
- Rubinstein Syndrome
- Syndrome, Rubinstein
- Broad Thumbs and Great Toes, Characteristic Facies, and Mental Retardation
- Broad Thumb-Hallux Syndrome
- Broad Thumb Hallux Syndrome
- Broad Thumb-Hallux Syndromes
- Syndrome, Broad Thumb-Hallux
- Syndromes, Broad Thumb-Hallux
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Below are MeSH descriptors whose meaning is more general than "Rubinstein-Taybi Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Rubinstein-Taybi Syndrome".
This graph shows the total number of publications written about "Rubinstein-Taybi Syndrome" by people in this website by year, and whether "Rubinstein-Taybi Syndrome" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2009 | 1 | 0 | 1 |
2010 | 1 | 0 | 1 |
2012 | 0 | 1 | 1 |
2014 | 1 | 0 | 1 |
2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Rubinstein-Taybi Syndrome" by people in Profiles.
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Opposing Effects of CREBBP Mutations Govern the Phenotype of Rubinstein-Taybi Syndrome and Adult SHH Medulloblastoma. Dev Cell. 2018 03 26; 44(6):709-724.e6.
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A patient with a de-novo deletion 3p25.3 and features overlapping with Rubinstein-Taybi syndrome. Clin Dysmorphol. 2014 Apr; 23(2):67-70.
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Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome. Am J Hum Genet. 2012 Feb 10; 90(2):308-13.
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Two patients with EP300 mutations and facial dysmorphism different from the classic Rubinstein-Taybi syndrome. Am J Med Genet A. 2010 Jan; 152A(1):181-4.
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Two adults with Rubinstein-Taybi syndrome with mild mental retardation, glaucoma, normal growth and skull circumference, and camptodactyly of third fingers. Am J Med Genet A. 2009 Dec; 149A(12):2849-54.