First case report of inherited Rubinstein-Taybi syndrome
Por um escritor misterioso
Last updated 07 julho 2024
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Background Rubinstein-Taybi syndrome (RSTS; OMIM #180849, #613684) is a rare autosomal dominant genetic condition characterized by broad thumbs and halluces, facial dysmorphism, short stature and variable degree of intellectual disability. RSTS is associated with mutations in CREBBP and EP300 genes in 50–60% and 5–8% of cases, respectively. The majority of cases are de novo heterozygous mutations. Case presentation Here we describe a familial RSTS case, associated with a novel EP300 mutation. The proband was a 9 years old female, with mild learning difficulties. Her mother, who also had learning difficulties, was found to have short and broad thumbs. MLPA and panel-based NGS of CREBBP and EP300 were performed. A novel heterozygous frameshift mutation in exon 31 of the EP300 gene (c.7222_7223del; p.(Gln2408Glufs*39)) was found in both. Conclusions This case represents the first case of inherited EP300-RSTS. The location of the frameshift deletion not affecting HAT domain and PHD finger, could explain the mild phenotype and the well-preserved intelligence. These patients are mildly affected, and this case highlights the possible missed diagnosis. We would recommend molecular testing of apparently healthy parents, and in the case of inherited mutations, of all adult first degree relatives at risk.
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PDF] Rubinstein-Taybi Syndrome Associated with Pituitary
![First case report of inherited Rubinstein-Taybi syndrome](https://europepmc.org/articles/PMC3948208/bin/nihms-552680-f0001.jpg)
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract
![First case report of inherited Rubinstein-Taybi syndrome](https://i1.rgstatic.net/publication/271223834_Rubinstein-Taybi_syndrome_Clinical_features_genetic_basis_diagnosis_and_management/links/54d25a210cf28e069723ee05/largepreview.png)
PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis
![First case report of inherited Rubinstein-Taybi syndrome](https://onlinelibrary.wiley.com/cms/asset/4eaba3ea-5380-4e9f-ab1c-05a6206fd2b1/mfig001.jpg)
Inheritance and variable expression in Rubinstein–Taybi syndrome
![First case report of inherited Rubinstein-Taybi syndrome](https://onlinelibrary.wiley.com/cms/asset/788505c9-dd5b-4ed2-bc06-19359d6eab1e/ajmga61888-fig-0002-m.jpg)
Rubinstein–Taybi syndrome in diverse populations - Tekendo
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Rubinstein-Taybi Syndrome: A Pediatric Case Report
![First case report of inherited Rubinstein-Taybi syndrome](https://www.ncbi.nlm.nih.gov/books/NBK1526/bin/rsts-Image002.jpg)
Figure 2. [Broad terminal phalanges (A) and broad, radially
![First case report of inherited Rubinstein-Taybi syndrome](https://jmg.bmj.com/content/jmedgenet/37/3/168/F2.large.jpg)
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids
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Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
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Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in
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