Genotype-phenotype correlations in Rubinstein-Taybi syndrome

• Published in: American journal of medical genetics. Part A 2008-10, Vol.146A (19), p.2512-2519
• Main Authors: Schorry, E.K., Keddache, M., Lanphear, N., Rubinstein, J.H., Srodulski, S., Fletcher, D., Blough-Pfau, R.I., Grabowski, G.A.
• Format: Article
• Language: English
• Subjects: Alternative Splicing - genetics; Amino Acid Substitution; autism; Autistic Disorder - genetics; Biological and medical sciences; Child clinical studies; Cohort Studies; CREB binding protein; CREB-Binding Protein - genetics; CREB-Binding Protein - metabolism; CREBBP; Developmental disorders; Diseases of the osteoarticular system; Exons; Gene Deletion; Genotype; Growth Disorders - genetics; growth retardation; In Situ Hybridization, Fluorescence; Infantile autism; Malformations and congenital and or hereditary diseases involving bones. Joint deformations; Medical genetics; Medical sciences; Mutation; Mutation, Missense; Phenotype; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Retrospective Studies; Rubinstein-Taybi syndrome; Rubinstein-Taybi Syndrome - diagnosis; Rubinstein-Taybi Syndrome - genetics
• ISSN: 1552-4825; 1552-4833
• DOI: 10.1002/ajmg.a.32424

Rubinstein–Taybi syndrome (RTS) is a rare multiple congenital anomaly/intellectual impairment syndrome. Loss of function in CREBBP or EP300 genes has been found in about 50% of patients with RTS. Genotype–phenotype correlations were investigated in 93 patients meeting diagnostic criteria for RTS during 2 international RTS family conferences. Mutation analysis of CREBBP was performed on all 31 coding exons and exon–intron junctions; a subset of patients had FISH analysis for large deletions. A total of 64 different variations were observed in the DNA sequence, and determined to be definitive mutations in 52 patients (56%). Mutations detected included: 10 missense mutations; 36 truncating or splice‐site mutations; and 6 large deletions detectable by FISH. Fourteen patients had synonymous changes of unknown significance. The majority of mutations affected the HAT domain of CREBBP or predicted termination of the protein before the HAT region. Extensive phenotypic data were collected on each patient and analyzed to determine correlations with mutation types, that is, truncating, large deletions, single amino acid substitutions, or no CREBBP mutation. All four groups displayed the characteristic facial and thumb dysmorphology. Growth retardation in height and weight was seen more frequently in patients with no CREBBP mutation; seizure disorder was more frequent in those with CREBBP mutations. Degree of mental retardation was similar in all groups, although there was a trend toward lower IQ and autistic features in patients with large deletions. Similarity in phenotype between the groups implies that the several genes involved in causing RTS likely have effects through the same pathway. © 2008 Wiley‐Liss, Inc.