Rubinstein-Taybi 2 associated to novel EP300 mutations: deepening the clinical and genetic spectrum.
María LópezAlberto García-OguizaJudith ArmstrongInmaculada García-CobaledaSixto García-MiñaurFernando Santos-SimarroVerónica SeidelMaría LópezPublished in: BMC medical genetics (2018)
The clinical evaluation of our patients corroborates that clinical features in EP300 are less marked than in CREBBP patients although it is difficult to establish a genotype-phenotype correlation although. It is remarkable that these findings are observed in a RSTS-diagnosed cohort; some patients harbouring EP300 mutations could present a different phenotype. Broadening the knowledge about EP300-RSTS phenotype may contribute to improve the management of patients and the counselling to the families.