Cargando…
Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report
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 followin...
Autores principales: | Al-Qattan, Mohammad M., Jarman, Abdulaziz, Rafique, Atif, Al-Hassnan, Zuhair N., Al-Qattan, Heba M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330443/ https://www.ncbi.nlm.nih.gov/pubmed/30635043 http://dx.doi.org/10.1186/s12881-019-0747-5 |
Ejemplares similares
-
Chromosome 16p13.3 Contiguous Gene Deletion Syndrome including the SLX4, DNASE1, TRAP1, and CREBBP Genes Presenting as a Relatively Mild Rubinstein–Taybi Syndrome Phenotype: A Case Report of a Saudi Boy
por: Al-Qattan, Mohammad M., et al.
Publicado: (2020) -
CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome
por: Wincent, Josephine, et al.
Publicado: (2015) -
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients
por: Bentivegna, Angela, et al.
Publicado: (2006) -
A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome
por: Wang, Qian, et al.
Publicado: (2022) -
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
por: Yumul, Rhea Camille R., et al.
Publicado: (2022)