Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Por um escritor misterioso
Last updated 16 junho 2024
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Background Rubinstein-Taybi syndrome (RSTS) Type 1 (OMIM 180849) is characterized by three main features: intellectual disability; broad and frequently angulated thumbs and halluces; and characteristic facial dysmorphism. Case presentation We report on a Saudi boy with RSTS Type 1 and the following distinct features: a midline notch of the upper lip, a bifid tip of the tongue, a midline groove of the lower lip, plump fingers with broad / flat fingertips, and brachydactyly. The child was found to be heterozygous in the CREBBP gene for a sequence variant designated c.4963del, which is predicted to result in premature protein termination p.Leu1655Cysfs*89. The child and his father were also found to be heterozygous in the EP300 gene for a sequence variant designated c.586A > G, which is predicted to result in the amino-acid substitution p.Ile196Val. Conclusion Our report expands the clinical spectrum of RSTS to include several distinct facial and limb features. The variant of the CREBBP gene is known to be causative of RSTS Type 1. The variant in the EP300 gene is benign since the father carried the same variant and exhibited no abnormalities. However, functional studies are required to investigate if this benign EP300 variant influences the phenotype in the presence of disease-causing CREBBP gene mutations.
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](https://i1.rgstatic.net/ii/profile.image/875824425222145-1585824223331_Q64/Atif-Rafique.jpg)
PDF) Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: A case report
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](http://faoj.org/wp-content/uploads/2008/06/rstsfig1a.jpg)
Rubinstein-Taybi Syndrome: A case report
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2Fs12920-023-01516-9/MediaObjects/12920_2023_1516_Fig1_HTML.png)
De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia, BMC Medical Genomics
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](https://ijdvl.com/content/126/2013/79/5/Images/ijdvl_2013_79_5_714_116751_f2.jpg)
Rubinstein-Taybi syndrome: A report of two siblings with unreported cutaneous stigmata - Indian Journal of Dermatology, Venereology and Leprology
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](https://www.frontiersin.org/files/Articles/1116919/fgene-14-1116919-HTML/image_m/fgene-14-1116919-g005.jpg)
Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](https://pbs.twimg.com/media/EbmyHP_XYAARHA4.jpg:large)
Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric #Genetics # syndrome / X
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](https://0.academia-photos.com/attachment_thumbnails/86592259/mini_magick20220528-8773-1ogw71o.png?1653724845)
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral postaxial polydactyly Corresponding author
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](https://media.springernature.com/m685/springer-static/image/art%3A10.1007%2Fs10875-020-00808-4/MediaObjects/10875_2020_808_Figa_HTML.png)
Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](https://www.researchgate.net/profile/Mario-Giuffre/publication/279387339/figure/fig3/AS:267595962122250@1440811257406/4-Newborn-with-Rubinstein-Taybi-syndrome-showing-microcephaly-frontal-bossing_Q320.jpg)
4 Newborn with Rubinstein-Taybi syndrome showing microcephaly, frontal
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](https://d3i71xaburhd42.cloudfront.net/ed0f7a1f21195adc8b3bf65659ba24794ad14381/2-Figure1-1.png)
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](https://www.researchgate.net/publication/265393298/figure/tbl1/AS:601747814875153@1520479267562/Rubinstein-Taybi-syndrome-Multisystem-involvement-and-its-clinical-implications.png)
Rubinstein-Taybi syndrome: Multisystem involvement and its clinical
![Rubinstein-Taybi syndrome in a Saudi boy with distinct features](https://ars.els-cdn.com/content/image/1-s2.0-S1110863012000316-gr3.jpg)
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
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