A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics

Background This study was to report a novel CREBBP mutation and phenotype in a child with Rubinstein–Taybi syndrome. Methods Case report of a 9-year-old boy. Results We described the patient’s clinical manifestations in detail, and found that in addition to the typical systemic manifestations of the syndrome, the outstanding manifestation of the child was severe intellectual deficiency and prominent ocular abnormalities. Whole-exome sequencing and sanger sequencing were performed on the patient and his parents, a large intragenic deletion, covering the exon 1 region and part of the intron 1 region of the TRAP1 gene, and the entire region from intron 27 to exon 30 of the CREBBP gene (chr16:3745393-3783894) was identified on the patient. This mutation affected the CREBBP histone acetyltransferase (HAT) domain. Conclusions This findings in our patient add to the spectrum of genetic variants described in Rubinstein–Taybi syndrome and present a RSTS patient with various ocular anomalies including early onset glaucoma.

Brain size regulations by cbp haploinsufficiency evaluated by in

PDF) Genetic heterogeneity in Rubinstein-Taybi syndrome

A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with

Ultra-Rare Syndromes: The Example of Rubinstein-Taybi Syndrome

High frequency of copy number imbalances in Rubinstein–Taybi

Distribution of CREBBP domains and mutations in our patient (in

Figure 2 from A case of Rubinstein-Taybi Syndrome with a CREB

Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With

High frequency of mosaic CREBBP deletions in Rubinstein–Taybi

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian

Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian