Rubinstein-Taybi Syndrome
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).
Year introduced: 1991(1972)
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Tree Number(s): C05.116.099.370.797, C05.660.207.850, C10.597.606.360.700, C16.131.077.804, C16.131.260.790, C16.131.621.207.850, C16.320.180.790
MeSH Unique ID: D012415
Entry Terms:
- Rubinstein Taybi Syndrome
- Syndrome, Rubinstein-Taybi
- Rubinstein Syndrome
- Syndrome, Rubinstein
- Broad Thumb-Hallux Syndrome
- Broad Thumb Hallux Syndrome
- Broad Thumb-Hallux Syndromes
- Syndrome, Broad Thumb-Hallux
- Syndromes, Broad Thumb-Hallux
- Broad Thumbs and Great Toes, Characteristic Facies, and Mental Retardation
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