ABSTRACT
Several changes in the behavioral phenotype arise with the growth of children affected by Cornelia de Lange Syndrome (CdLS) and Rubinstein-Taybi Syndrome (RSTS). However, previous research relied on a cross-sectional study design turning into age-related comparisons of different syndromic cohorts to explore age-dependent changes. We aim to outline the variating pathways of the neuropsychiatric functioning across the lifespan in CdLS and RSTS, through the setting up of a longitudinal study design. The sample included 14 patients with CdLS and 15 with RSTS. The assessments were carried out in two different timepoints. Our findings highlight that the cognitive profile of CdLS is subjected to a worsening trend with decreasing Intellectual Quotient (IQ) scores from T0 to T1, whereas RSTS shows a stable IQ over time. Patients affected by RSTS show greater improvements compared to CdLS in communication, daily living skills, social abilities, and motor skills across the lifespan. Both syndromes report an upward trend in behavioral and emotional difficulties even if CdLS exhibit a significant and major deterioration compared to individuals with RSTS. Being aware of the early dysfunctional patterns which might pave the way for later neuropsychiatric impairments is the first step for planning preventive interventions.
Subject(s)
De Lange Syndrome , Rubinstein-Taybi Syndrome , Humans , Rubinstein-Taybi Syndrome/genetics , Rubinstein-Taybi Syndrome/psychology , Longitudinal Studies , Cross-Sectional Studies , De Lange Syndrome/diagnosis , De Lange Syndrome/genetics , PhenotypeABSTRACT
BACKGROUND AND AIM: There is mounting evidence highlighting that Cornelia de Lange Syndrome (CdLS) and Rubinstein-Taybi Syndrome's (RSTS) behavioral phenotypes are not stable over individual developmental trajectories and that several psychiatric disorders might arise with age. Our study aims to examine the specific hallmarks of psychopathology and behavioral phenotypes in four different age ranges: infancy and toddlerhood, early childhood, middle childhood, and adolescence, in both genetic syndromes. METHOD: The sample included 44 patients with CdLS (48% boys, age = 6.67 ± 4.36) and 31 with RSTS (48% boys, age = 6.89 ± 4.58) recruited through follow-ups. Cognitive, behavioral, and autism assessments were carried out with Griffith's scales or the Leiter-R, the Child Behavior Checklist, and the Child Autism Rating Scales 2. Multiple ANOVA 2 × 4 were run to outline behavioral phenotypic age-related syndromic markers and ANCOVA to value the weight of IQ and ASD-related traits on the psychopathological outcome. RESULTS: Findings showed that anxiety is a crucial phenotypic hallmark, independent of IQ but associated with autistic traits, that increases from infancy to adolescence in both CdLS and RSTS. CONCLUSION AND IMPLICATIONS: Being aware of the developmental challenges that growing children are called to face is essential for drawing up proper standards of assessment turning into target age-related interventions, ensuring these patients personalized healthcare and improvement in life quality.
Subject(s)
Autistic Disorder , De Lange Syndrome , Fragile X Syndrome , Mental Disorders , Rubinstein-Taybi Syndrome , Child , Child, Preschool , De Lange Syndrome/genetics , De Lange Syndrome/psychology , Female , Fragile X Syndrome/psychology , Humans , Male , Rubinstein-Taybi Syndrome/genetics , Rubinstein-Taybi Syndrome/psychologyABSTRACT
The journey to receiving a diagnosis for rare genetic disease can be long and emotionally impactful. This study describes parental experiences of receiving their child's diagnosis of Rubinstein-Taybi syndrome (RTS), a rare genetic condition characterized by growth and developmental delay together with dysmorphic features. Parents from the RTS Australia support group participated in qualitative, semi-structured phone interviews, which were transcribed verbatim and thematically analyzed. Questions focused on psychosocial challenges and benefits pre and post-diagnosis. Ten mothers and three fathers participated, with the mean age of diagnosis being 8 months. Parents reported positive psychological effects from a slight delay in diagnosis, and negative effects from an extended diagnostic delay, suggesting the ideal time for a parent to receive a diagnosis lies in the post attachment stage, prior to the development of significant parental concerns. This stage would vary depending on condition severity. Parents desired a diagnosis to reduce uncertainty; however, uncertainty remained post diagnosis, and shifted its focus from broadly encompassing etiology and prognosis, to specifically focusing on concerns regarding severity within the spectrum. Perceived benefits of a diagnosis mainly centered on the provision of a label. Parents articulated that a label increased social acceptance, enhanced coping, promoted communication, and improved access to medical, financial, and support services. This study provides insights into the experience of families prior to and following receipt of a diagnosis. It also highlights the possibility of an optimal time window to receive a diagnosis; in which bonding is maximized and parental distress is minimized.
Subject(s)
Delayed Diagnosis/psychology , Parents/psychology , Rare Diseases/diagnosis , Rubinstein-Taybi Syndrome/diagnosis , Adaptation, Psychological , Australia/epidemiology , Body Dysmorphic Disorders/diagnosis , Body Dysmorphic Disorders/epidemiology , Body Dysmorphic Disorders/genetics , Body Dysmorphic Disorders/psychology , Child , Child, Preschool , Developmental Disabilities/diagnosis , Developmental Disabilities/epidemiology , Developmental Disabilities/genetics , Developmental Disabilities/psychology , Fathers/psychology , Female , Humans , Infant , Male , Rare Diseases/epidemiology , Rare Diseases/genetics , Rare Diseases/psychology , Rubinstein-Taybi Syndrome/epidemiology , Rubinstein-Taybi Syndrome/genetics , Rubinstein-Taybi Syndrome/psychology , Self-Help GroupsABSTRACT
We directly assessed the broader aspects of sociability (social enjoyment, social motivation, social interaction skills and social discomfort) in individuals with Cornelia de Lange (CdLS), fragile X (FXS) and Rubinstein-Taybi syndromes (RTS), and their association with autism characteristics and chronological age in these groups. Individuals with FXS (p < 0.01) and RTS (p < 0.01) showed poorer quality of eye contact compared to individuals with CdLS. Individuals with FXS showed less person and more object attention than individuals with CdLS (p < 0.01). Associations between sociability and autism characteristics and chronological age differed between groups, which may indicate divergence in the development and aetiology of different components of sociability across these groups. Findings indicate that individuals with CdLS, FXS and RTS show unique profiles of sociability.
Subject(s)
De Lange Syndrome/psychology , Fragile X Syndrome/psychology , Rubinstein-Taybi Syndrome/psychology , Social Interaction , Social Skills , Adolescent , Adult , Child , Child, Preschool , Cross-Sectional Studies , De Lange Syndrome/diagnosis , Female , Fragile X Syndrome/diagnosis , Humans , Male , Middle Aged , Motivation/physiology , Pleasure/physiology , Rubinstein-Taybi Syndrome/diagnosis , Young AdultABSTRACT
Unique socio-behavioural phenotypes are reported for individuals with different neurodevelopmental disorders. Here, the effects of adult familiarity and nature of interaction on social anxiety and social motivation were investigated in individuals with fragile X (FXS; n = 20), Cornelia de Lange (CdLS; n = 20) and Rubinstein-Taybi (RTS; n = 20) syndromes, compared to individuals with Down syndrome (DS; n = 20). The Social Anxiety and Motivation Rating Scale was employed whilst participants completed four social tasks, each administered separately by a familiar adult, and also by an unfamiliar adult. Compared to participants with DS, those with FXS and RTS exhibited high levels of social anxiety but similar levels of social motivation. Participants with CdLS showed heightened social anxiety and reduced social motivation only during interactions with an unfamiliar adult when active participation was voluntary.
Subject(s)
De Lange Syndrome/psychology , Down Syndrome/psychology , Fragile X Syndrome/psychology , Motivation , Phobia, Social , Rubinstein-Taybi Syndrome/psychology , Social Behavior , Adult , Female , Humans , Male , Young AdultABSTRACT
Anxiety disorders are heightened in specific genetic syndromes in comparison to intellectual disability of heterogeneous aetiology. In this study, we described and contrasted anxiety symptomatology in fragile X (FXS), Cornelia de Lange (CdLS) and Rubinstein-Taybi syndromes (RTS), and compared the symptomatology to normative data for typically-developing children and children diagnosed with an anxiety disorder. Scores did not differ between children diagnosed with an anxiety disorder and (a) participants with FXS on social phobia, panic/agoraphobia, physical injury fears, and obsessive-compulsive subscales (b) participants with CdLS on separation anxiety, generalized anxiety, panic/agoraphobia, physical injury fears and obsessive-compulsive subscales, and (c) participants with RTS on panic/agoraphobia and obsessive-compulsive subscales. The results highlight divergent profiles of anxiety symptomatology between these groups.
Subject(s)
Anxiety Disorders/psychology , De Lange Syndrome/psychology , Fragile X Syndrome/psychology , Rubinstein-Taybi Syndrome/psychology , Adolescent , Adult , Anxiety Disorders/diagnosis , Anxiety Disorders/genetics , Child , De Lange Syndrome/diagnosis , De Lange Syndrome/genetics , Female , Fragile X Syndrome/diagnosis , Fragile X Syndrome/genetics , Humans , Intellectual Disability/diagnosis , Intellectual Disability/genetics , Intellectual Disability/psychology , Male , Rubinstein-Taybi Syndrome/diagnosis , Rubinstein-Taybi Syndrome/genetics , Young AdultABSTRACT
Few comparative studies have evaluated the heterogeneity of sociability across a range of neurodevelopmental disorders. The Sociability Questionnaire for People with Intellectual Disability (SQID) was completed by caregivers of individuals with Cornelia de Lange (n = 98), Angelman (n = 66), Fragile X (n = 142), Down (n = 117) and Rubinstein Taybi (n = 88) syndromes and autism spectrum disorder (ASD; n = 107). Between groups and age-band (<12yrs; 12-18yrs; >18yrs) comparisons of SQID scores were conducted. Rates of behaviors indicative of selective mutism were also examined. Fragile X syndrome achieved the lowest SQID scores. Cornelia de Lange, ASD, and Fragile X groups scored significantly lower than Angelman, Down and Rubinstein Taybi groups. Selective mutism characteristics were highest in Cornelia de Lange (40%) followed by Fragile X (17.8%) and ASD (18.2%). Age-band differences were identified in Cornelia de Lange and Down syndrome.
Subject(s)
Angelman Syndrome/psychology , Autism Spectrum Disorder/psychology , De Lange Syndrome/psychology , Down Syndrome/psychology , Fragile X Syndrome/psychology , Rubinstein-Taybi Syndrome/psychology , Social Skills , Adolescent , Child , Female , Humans , Male , Surveys and QuestionnairesABSTRACT
OBJECT: Rubinstein-Taybi syndrome (RSTS) is a rare condition with characteristic genetic and clinical features. The presence of variable vertebral and neural axis abnormalities has been reported in the literature. We describe the possible association of multiple different spinal anomalies in these patients. RESULTS: The radiological exams of two RSTS patients (a female and male of 11 and 13 years) have been reviewed. Both patients presented the simultaneous association of craniovertebral junction bony abnormalities (occipito-C1 condyle subluxation and posterior C2-C3 arches fusion), Chiari I malformation, spinal cord syrinx, low-lying conus medullaris, and scoliosis. CONCLUSION: An association of different spinal cord anomalies is possible in RSTS patients and has to be investigated with a comprehensive neuroimaging study in order to address the proper treatment and prevent the development of neurologic deficits.
Subject(s)
Cervical Vertebrae/abnormalities , Rubinstein-Taybi Syndrome/pathology , Scoliosis/pathology , Arnold-Chiari Malformation/pathology , Child , Cyclic AMP Response Element-Binding Protein/genetics , Female , Humans , Image Processing, Computer-Assisted , Intellectual Disability/etiology , Magnetic Resonance Imaging , Male , Mutation/genetics , Mutation/physiology , Neurologic Examination , Rubinstein-Taybi Syndrome/psychology , Spinal Cord Compression/complications , Spinal Cord Compression/pathology , Spine/abnormalities , Spine/pathology , Syringomyelia/complications , Syringomyelia/pathology , Tomography, X-Ray ComputedABSTRACT
BACKGROUND: The diagnosis of Rubinstein-Taybi syndrome (RTS) is primarily clinical and based on the characteristic phenotype that is often combined with a variety of somatic anomalies and psychiatric disorders. SAMPLING AND METHODS: In this paper, a review is presented of the psychiatric and behavioural aspects of RTS. This is illustrated with a case report. RESULTS: Behavioural aspects of about 150 patients are described, and include a variable degree of mental retardation, impulsivity, distractibility, instability of mood and stereotypies. In general, patients with RTS are described as sociable and friendly. Information about brain pathology is virtually absent. In about half of the cases, the syndrome is caused by a mutation or deletion of the CREB-binding protein (CBP) gene (16p13.3). The case report deals with an adult male who was referred for impulsivity and temper outbursts. A provisional diagnosis of atypical depression was made, and treatment with citalopram resulted in a remarkable amelioration of his mood and behaviour that persisted for more than 2 years (last observation). CONCLUSION: Patients with undetected genetic syndromes do occur in clinical psychiatry, and the clinician has to consider such disorders in cases with disturbed development, dysmorphias and somatic comorbidity.
Subject(s)
Depressive Disorder/diagnosis , Depressive Disorder/psychology , Disruptive, Impulse Control, and Conduct Disorders/diagnosis , Disruptive, Impulse Control, and Conduct Disorders/psychology , Intellectual Disability/diagnosis , Intellectual Disability/psychology , Rubinstein-Taybi Syndrome/diagnosis , Rubinstein-Taybi Syndrome/psychology , Adult , CREB-Binding Protein/genetics , Chromosome Deletion , Chromosomes, Human, Pair 22/genetics , DNA Mutational Analysis , Depressive Disorder/genetics , Diagnosis, Differential , Disruptive, Impulse Control, and Conduct Disorders/genetics , E1A-Associated p300 Protein/genetics , Humans , Intellectual Disability/genetics , Male , Neuropsychological Tests/statistics & numerical data , Phenotype , Psychometrics , Rubinstein-Taybi Syndrome/geneticsABSTRACT
Research regarding the behavioral aspects of children with Rubinstein-Taybi syndrome (RTS) has suggested some possible behavioral patterns including autistic features. Caregivers of 39 children (mean age = 8.4 years) with RTS (49% showing abnormality in CREBBP gene) and 39 children (mean age = 8.6 years) matched on developmental level, age and gender were administered the Child Behavior Checklist and the Children's Social Behavior Questionnaire. Children with RTS did not exhibit higher internalizing (affective and anxiety symptoms) or externalizing (disruptive symptoms) behavioral problems than expected for their age/developmental range. However, they displayed some specific behaviors: short attention span, motor stereotypies, poor coordination, and overweight. The presence of an identified CREBBP gene abnormality was possibly related to the motor difficulties through impaired motor skills learning.
Subject(s)
Autistic Disorder/diagnosis , Autistic Disorder/genetics , CREB-Binding Protein/genetics , Child Behavior Disorders/diagnosis , Child Behavior Disorders/genetics , Psychomotor Disorders/diagnosis , Psychomotor Disorders/genetics , Rubinstein-Taybi Syndrome/diagnosis , Rubinstein-Taybi Syndrome/genetics , Social Behavior , Adolescent , Autistic Disorder/psychology , Child , Child Behavior Disorders/psychology , DNA Mutational Analysis , Female , Humans , Male , Overweight/diagnosis , Overweight/genetics , Overweight/psychology , Personality Assessment/statistics & numerical data , Phenotype , Psychometrics , Psychomotor Disorders/psychology , Rubinstein-Taybi Syndrome/psychology , Stereotyped BehaviorABSTRACT
A mouse model of Rubinstein-Taybi syndrome (RTS) was generated by an insertional mutation into the cyclic AMP response element-binding protein (CREB)-binding protein (CBP) gene. Heterozygous CBP-deficient mice, which had truncated CBP protein (residues 1-1084) containing the CREB-binding domain (residues 462-661), showed clinical features of RTS, such as growth retardation (100%), retarded osseous maturation (100%), hypoplastic maxilla with narrow palate (100%), cardiac anomalies (15%) and skeletal abnormalities (7%). Truncated CBP is considered to have been acting during development as a dominant-negative inhibitor to lead to the phenotypes of RTS in mice. Our studies with step-through-type passive avoidance tests and with fear conditioning test showed that mice were deficient in long-term memory (LTM). In contrast, short-term memory (STM) appeared to be normal. These results implicate a crucial role for CBP in mammalian LTM. Our CBP +/- mice would be an excellent model for the study of the role of CBP in development and memory storage mechanisms.
Subject(s)
Nuclear Proteins/genetics , Rubinstein-Taybi Syndrome/genetics , Trans-Activators/genetics , Animals , Base Sequence , Behavior, Animal , CREB-Binding Protein , DNA Primers/genetics , Disease Models, Animal , Female , Genes, Dominant , Heterozygote , Humans , Male , Memory , Mice , Mice, Mutant Strains , Motor Activity/genetics , Mutagenesis, Insertional , Phenotype , Pregnancy , Rubinstein-Taybi Syndrome/pathology , Rubinstein-Taybi Syndrome/psychology , Sequence DeletionABSTRACT
In 1963 Rubinstein and Taybi described a new syndrome characterized by broad thumbs and toes, facial abnormalities and mental retardation. The syndrome can be observed in the neonatal period by typical thumbs, halluces and facial abnormalities. The prevalence in the general population is unknown, however the disorder is not rare and is present in about 1:600 patients in mental retardation clinics. At the present time there is no definite inheritance pattern and recurrence is very unlikely. 18 different chromosomal anomalies have been identified in some patients with this syndrome. In this paper we identify a typical case and review the symptoms and signs of the RT syndrome and meta-analyze 732 cases.
Subject(s)
Rubinstein-Taybi Syndrome/genetics , Adolescent , Child , Child, Preschool , Humans , Infant , Infant, Newborn , Rubinstein-Taybi Syndrome/pathology , Rubinstein-Taybi Syndrome/psychologyABSTRACT
Forty individuals with Rubinstein-Taybi syndrome were tested using an extensive test battery to obtain more insight about their intelligence level, social competency, temperament, and behavior as well as articulation and receptive and expressive language level. Examination of individuals in the Netherlands who have this rare syndrome has been extensive, allowing some generalizations to be made. The intelligence level of affected individuals is usually low, although some persons have much higher scores than do others. The tested individuals were remarkably consistent in their social competency, temperament, and behavior. They were able to make good use of their limited verbal abilities. Comparable studies of other groups of persons with a specific syndrome are needed to determine whether the present findings are specific for Rubinstein-Taybi syndrome or may be found among persons with other syndromes.
Subject(s)
Articulation Disorders/psychology , Language Development Disorders/psychology , Rubinstein-Taybi Syndrome/psychology , Adolescent , Adult , Articulation Disorders/diagnosis , Child , Child, Preschool , Female , Humans , Language Development Disorders/diagnosis , Language Tests , Male , Neuropsychological Tests , Rubinstein-Taybi Syndrome/diagnosis , Social Adjustment , Speech Production MeasurementABSTRACT
The article presents the results of clinicogenetic studies of two syndromal forms of complicated oligophrenia featuring the intellectual underdevelopment combined with apraxic cortical dysarthria, hypogenitalism and multiple dysontogenies. Psychopathological structure of these syndromal forms of complicated oligophrenia are given. This is of major importance for diagnostic, medical and psycho-pedagogical correction. The questions of genetic heterogeneity of the syndromes are discussed.
