Rubinstein-Taybi syndrome in a Saudi boy with distinct features

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Last updated 22 dezembro 2024
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
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
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Clinical photos of the patients. (a) Case 1: Dysmorphic facial features
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
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
Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural tube defect. - Abstract - Europe PMC
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management, Italian Journal of Pediatrics
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Rubinstein-Taybi Syndrome 1
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
An Egyptian patient with Rubinstein-Taybi syndrome. Facial features
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Facial features of Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
The - The Rubinstein-Taybi Syndrome Children's Foundation
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Benign and malignant tumors in Rubinstein–Taybi syndrome - Boot - 2018 - American Journal of Medical Genetics Part A - Wiley Online Library
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
PDF) Lacrimal drainage anomalies in Rubinstein-Taybi syndrome: case report and review of literature
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Frontiers Case report: A preterm infant with rubinstein-taybi syndrome and Marmorata telangiectatica harboring a frameshift mutation in the CREBBP gene
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Rubinstein-Taybi Syndrome Images — DermNet
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
First case of Rubinstein–Taybi syndrome with desquamation associated with a novel mutation in the bromodomain of the CREBBP gene - Wang - 2019 - Clinical and Experimental Dermatology - Wiley Online Library

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