Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf
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Rubinstein-Taybi syndrome (RSTS) is characterized by distinctive facial features, broad and often angulated thumbs and halluces, short stature, and moderate-to-severe intellectual disability. Characteristic craniofacial features include downslanted palpebral fissures, low-hanging columella, high palate, grimacing smile, and talon cusps. Prenatal growth is often normal, then height, weight, and head circumference percentiles rapidly drop in the first few months of life. Short stature is typical in adulthood. Obesity may develop in childhood or adolescence. Average IQ ranges between 35 and 50; however, developmental outcome varies considerably. Some individuals with EP300-related RSTS have normal intellect. Additional features include ocular abnormalities, hearing loss, respiratory difficulties, congenital heart defects, renal abnormalities, cryptorchidism, feeding problems, recurrent infections, and severe constipation.
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Rubinstein–Taybi syndrome - Wikipedia
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High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis
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Approach to inherited hypertrichosis: A brief review - Indian Journal of Dermatology, Venereology and Leprology
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Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
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Genes, Free Full-Text
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Approach to inherited hypertrichosis: A brief review - Indian Journal of Dermatology, Venereology and Leprology
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genereviews.org - GeneReviews® - NCBI Bookshelf
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Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf
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JCM, Free Full-Text
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Rubinstein-Taybi syndrome with scoliosis treated with single-stage posterior spinal fusion: illustrative case in: Journal of Neurosurgery: Case Lessons Volume 1 Issue 11 (2021) Journals
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Figure 3. [Broad, partially duplicated halluces]. - GeneReviews® - NCBI Bookshelf
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Quality of life of Brazilian families who have children with Rubinstein–Taybi syndrome: An exploratory cross‐sectional study - Vale - 2022 - American Journal of Medical Genetics Part A - Wiley Online Library
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