- Open Access
A national survey of Rett syndrome: behavioural characteristics
© Cianfaglione et al.; licensee BioMed Central. 2015
Received: 13 November 2014
Accepted: 4 February 2015
Published: 4 March 2015
The aim was to gain a UK national sample of people with Rett syndrome (RTT) across the age range and compare their characteristics using a variety of relevant behavioural measures with a well-chosen contrast group.
The achieved sample was 91 girls and women, aged from 4 to 47 years, of whom 71 were known to be MECP2 positive. The contrast group (n = 66), matched for age, gender, language and self-help skills, comprised individuals with six other syndromes associated with intellectual disability. Parental questionnaire measures of RTT specific characteristics, impulsivity, overactivity, mood, interest and pleasure, repetitive behaviour and self-injury were administered.
Hand stereotypies, breathing irregularities, night-time unrest and anxiety or inappropriate fear were commonly reported among the RTT sample. Problems of low mood were also reported as common. However, mood and interest and pleasure were no lower than found in the contrast group. In addition, self-injury was lower than in the contrast group and was associated with factors found to predict self-injury in other groups of people with severe intellectual disabilities.
There is variability in the manifestation of problem behaviours potentially associated with the syndrome across individuals, with some more severely affected in most areas than others. Some of this variability appears to be underpinned by genetic mutation.
Rett syndrome (RTT) is a genetic disorder that causes severe cognitive and physical impairments. In its classic form, it appears to affect almost exclusively females, with an incidence of up to one in every 10,000 live female births. Its cause is most often a mutation in the methyl-CpG binding protein-2 (MECP2) gene, located on the X chromosome at Xq28 . However, although a MECP2 mutation is found in most cases of the classic form, RTT remains a clinical rather than a molecular diagnosis. MECP2 mutations have not been found in all cases of RTT, and mutation has been found in individuals who do not meet the clinical diagnostic criteria for classic or variant RTT .
Neul et al.  described revised diagnostic criteria. Classic RTT requires apparently normal psychomotor development in the first 6 months of life followed by a period of regression, which is not due to brain injury secondary to trauma, neurometabolic disease or severe infection, and involves partial or complete loss of acquired purposeful hand skills and language, gait abnormalities and the development of stereotypic hand movements, followed by stabilization or even some degree of recovery. An important aspect of the regression is a period of social withdrawal or impaired communication. Atypical RTT requires a similar period of regression and subsequent stabilization/recovery, at least two of the above four behavioural manifestations and the presence of at least five (out of 11) supportive criteria. Other variant forms have also been described .
Behavioural commonalities between surveys of RTT syndrome
Percentage of sample with characteristic
Coleman et al. [ 8 ]
Samson et al. [ 9 ]
Mount et al. [ 6 ]
Cass et al. [ 10 ]
Halbach et al. [ 11 ]
( N = 63)
( N = 107)
( N = 38)
( N = 87)
( N = 53)
( N = 91)
Low mood/mood changes
However, the existing literature has some limitations. First, RTT is rare and survey sizes are necessarily small. There is a need for further research to increase the evidence base. Second, there is a greater representation of children than adults in existing surveys. There is a need for further research on the behavioural characteristics of adults and on developmental trajectory into adulthood. Third, studies lack well-matched contrast groups in comparison to which a distinctive behavioural phenotype might be established. Fourth, certain behaviours, such as impulsivity, overactivity and withdrawal have received relatively less research attention. Impulsivity and overactivity are important to explore in those with severe or profound intellectual disability for their association with self-injury and aggression . Depression in RTT has never been researched. Its assessment in this group is a challenge due to characteristic profound intellectual disability and the associated inability to self-report feelings and emotions. One approach is to assess the presence of abnormally low mood and lack of interest [13,14].
The purpose here was, therefore, to gain a UK national sample of people with Rett syndrome across the age range, use a variety of relevant behavioural measures and compare their characteristics with a contrast group, controlled for gender, age, language and functional ability.
Before commencing the study, ethical approval was granted by the Research Ethics Committee for Wales (Application number: 09/MRE09/50).
The survey methodology is described in greater detail in Cianfaglione et al. . In brief, families were recruited through the British Isle Rett Syndrome Survey (BIRSS), an on-going database now maintained by AC at Cardiff University. Families (308) with a daughter or son with RTT were approached and 126 (40.9%) returned a consent form. Questionnaire packs were then distributed and families were contacted first by telephone and then by letter if they had not returned the questionnaires within 2 months from receiving them. Ninety-three families returned completed questionnaires (30.2% of the original 308, 73.8% of those who consented to take part). Ninety-two participants with RTT were female and one was male. The male participant was excluded from the final sample. One participant passed away during the study and was not included in the analysis.
The achieved sample comprised 91 girls and women with a diagnosis of RTT, of whom 80 (87.9%) lived at home and 11 (12.1%) lived in out of family placements. The sample was skewed towards people living in the family home as another research aim was to investigate the well-being of parents caring for a child with RTT (although this survey sought to include only individuals living with their parents, the information on the BIRSS database was not entirely up-to-date and a minority no longer did so). Ages ranged from 4 to 47 years with a mean of 20.5 years: 43 participants were children and 48 adults. Sixty nine had classic RTT (75.8%), 19 atypical RTT (20.9%) and three a MECP2-related disorder (4.3%). Seventy one were known to be MECP2 positive (78.0%): 52 in the classic group and 16 in the atypical group in addition to the three with MECP2-related disorder. Diagnosis of RTT was made by a pediatrician in 42.9% of cases, a clinical geneticist in 26.4%, by both a pediatrician and clinical geneticist in 3.3% and by another professional in 25.3% (this information was missing for the remaining 2.2%). Median age of diagnosis was 3.0 years (range, 1 to 39 years). Diagnosis occurred most commonly between 2 and 4 years of age.
Regression was reported in 87 (95.6%). In one case (1.1%), the mother was not sure if the child had had a regression and, in 3 others (3.3%), all with MECP2-related disorder, they reported that the child did not have a regression. Mean age of regression was 18.9 months (range, 6 to 84 months; SD 11.75): 15 (16.5%) had a regression before 12 months, 49 (53.8%) between 12 and 18 months, 18 (19.0%) between 19 and 36 months and 5 (5.5%) after 36 months (including, one participant who had a late regression at 7 years).
The Cerebra Centre, University of Birmingham, has gathered behavioural data over many years on individuals with intellectual disability associated with a variety of genetic syndromes other than RTT [16,17]. Access to these data enabled a contrast group (n = 66) to be selected that closely matched the RTT sample. Groups were matched on (a) gender, (b) chronological age, (c) mobility, (d) the self-help skills of feeding, washing and dressing and (e) use of words. The latter was a key matching criterion and only individuals with no verbal ability were included. Hence, the three individuals in the RTT sample with preserved verbal ability were excluded from the comparison made to the contrast group, reducing the RTT group to 88 for this aspect of the analysis. In other respects, all participants were female. On average, the RTT sample were 20.3 years old (SD 10.2; range, 4 to 47 years) and the contrast group 15.0 years old (SD 10.0; range, 4 to 45 years). Fifty percent of the RTT group were mobile independently compared to 53.0% of the contrast group. Just a third of the RTT sample (37.5%) could feed themselves with help compared to 68.2% of the contrast group. No-one in either the RTT sample or contrast group could feed themselves independently or wash or dress themselves either independently or with help.
The contrast group comprised individuals with Cornelia de Lange syndrome (N = 26, 39.4%), Angelman syndrome (N = 25, 37.9%), Cri du Chat syndrome (N = 5, 7.6%), 1p36 deletion syndrome (N = 7, 10.6%), Smith Magenis syndrome (N = 2, 3.0%) and Prader Willi syndrome (N = 1, 1.5%).
Families were asked to complete two questionnaire packs. One questionnaire pack related to the person with RTT, covering their early development, current skills, health and behavioural characteristics. The second questionnaire pack related to various aspects of family experience. It is some of the first set of measures that are of concern here. Most of the chosen measures had been developed and used by the Cerebra Centre in their research. However, the first two measures listed below were RTT specific and were, therefore, not available for the contrast group.
Simplified severity score
In the simplified severity score , information was requested about six features of RTT (sitting, walking, hand use, speech, epilepsy and spine deformation). Each domain is scored from 0 to 3, where 0 indicates a normal situation, 1 indicates impaired ability to sit and walk, reduced hand use, some words, epilepsy is controlled with medication and scoliosis is mild; 2 indicates that the abilities to sit, walk, use hands and speak are lost, epilepsy is uncontrolled and scoliosis is severe; 3 indicates that the individual never acquired the abilities to sit, walk, use hands and speak, status epilepticus occurs and scoliosis has been operated upon. The severity score evaluates the overall severity of the syndrome and indicates domains that are considered to influence evolution and severity in the long term. However, it is not sensitive to progression of the syndrome over time. The maximum score is 18. Cases with a score less than 9 are considered mild or less severe.
Rett syndrome behavioural questionnaire
The Rett Syndrome Behavioural Questionnaire (RSBQ)  is a 45-item checklist developed to assess behavioural and emotional characteristics of RTT. Items are rated 0 to 2, where 0 indicates that the behaviour is not true, 1 sometimes true and 2 often true. The scale is divided into eight subscales: General Mood, Breathing Abnormalities, Hand Behaviours, Repetitive Face Movements, Body Rocking and Expressionless Face, Night-time Behaviour, Fear/Anxiety and Walking/Standing. High internal consistency has been reported for the total score (>0.90) and eight subscales (0.60 to 0.79), with good inter-rater and test-retest reliability scores (total score, >0.80; subscales, 0.60 to 0.79) .
The Activity Questionnaire (AQ)  is an informant-based questionnaire that measures the frequency of impulsivity and overactivity behaviour in children and adults with intellectual disabilities, with or without verbal communication and mobility. It contains 18 questions (for example, Does your child wriggle or squirm about when seated or laying down? Does your child find it difficult holding still?) rated on a five-point Likert scale, where 0 indicates never or almost never, 1 some of the time, 2 half of the time, 3 a lot of the time and 4 always or almost all the time. Behavioural features are clearly described and the respondent is asked to rate the frequency of each behaviour in the last 4 weeks. The scale is divided into three subscales: Overactivity, Impulsivity and Impulsive Speech.
Immobile and non-verbal individuals are scored differently from those who can walk and/or speak. Scores on the Impulsivity subscale for non-mobile individuals are pro-rated to compare with those for mobile individuals. Good internal consistency, item level inter-rater reliability score ranges of 0.31 to 0.75 (mean 0.56) and test re-test reliability score ranges of 0.60 to 0.90 (mean 0.75) have been reported across the subscales .
Mood, interest and pleasure questionnaire short-form
The Mood, Interest and Pleasure Questionnaire Short-Form (MIPQ-S)  assesses mood, interest and pleasure levels in individuals with severe and profound intellectual disability. It contains 12 items scored using a five-point Likert scale based on the respondents’ observation of the participant in the last 2 weeks. High scores indicate positive mood and high interest and pleasure. There are two subscales: Mood and Interest and Pleasure. Scores up to and including 15 and 6 (≤18 years) and 13 and 6 (>18 years) have been identified as being abnormally low and scores equal to or above 24 and 23 (≤18 years) and 24 and 21 (<18 years) as being abnormally high for the two subscales, respectively . Inter-rater and test-retest reliability scores have been reported as good (0.85 and 0.97 respectively) as has internal consistency (Cronbach’s alpha coefficient Total = 0.88, Mood = 0.79, Interest and Pleasure = 0.87) .
Repetitive behaviour questionnaire
The Repetitive Behaviour Questionnaire (RBQ)  is a 19-item informant-based scale used to assess repetitive behaviour in individuals with intellectual disability. It has five subscales: Stereotyped Behaviour, Compulsive Behaviour, Restricted Preferences, Repetitive Use of Language, and Insistence on Sameness. However, the Repetitive Use of Language and Restricted Preferences subscales cannot be scored for individuals with no language as items require the person to be verbal. The frequency of behaviour on each item is scored on a five-point Likert scale (0 to 4). Two scoring systems can be applied for verbal (total score range, 0 to 76) and non-verbal individuals (total score range, 0 to 60). Items that are dependent on the person being verbal can be excluded when comparing verbal and non-verbal individuals. Clinical cut-offs for each subscale are reached if the individual scores three or more on at least one item (that is, a behaviour occurs ‘once a day’ or ‘more than once a day’). Inter-rater reliability scores ranging from 0.46 to 0.80 at item level and test-retest reliability scores ranging from 0.61 to 0.93 at item level have been reported . The following internal consistency coefficients have been reported: full-scale level > .80, the stereotyped behavior and compulsive behavior subscales both > .70, restricted preferences, repetitive speech and insistence on sameness subscales .50, .54 and .65, respectively .
Challenging behaviour questionnaire
The Challenging Behaviour Questionnaire (CBQ)  is an informant-based scale that assesses the presence and frequency of self-injury and aggressive behaviour. Respondents are asked to rate the presence of self-injury and aggression in the last month and to specify the topography of the self-injurious behaviour (hitting self, bites self, slap, bangs head, pulls hair or skin, rubs or scratches self, inserts finger or objects in self). Psychometric properties of the scale are considered to be good with inter-rater reliability coefficients ranging from 0.61 to 0.89 .
For a few participants, some questionnaire items were missing even after attempting to complete them by contacting the respondents by telephone or using relevant information provided in response to another question. Guidelines from questionnaire manuals were employed for pro-rating missing data. Where the missing items were part of a scale or subscale, the mean for the scale/subscale was substituted, providing that 75% of items were scored for the MIPQ and AQ, 65% of items in each subscale were rated for the RBQ and 90% of items were rated for the RSBQ. Having done this, one case was excluded from the analysis of both the RSBQ and AQ and two from the analysis of the MIPQ due to missing data.
Total and subscale mean scores for the RSBQ, AQ, MIPQ and RBQ were calculated. Two sets of analyses were then pursued: (a) testing to establish differences between the RTT sample and the contrast group, and (b) exploration of variation within the RTT group in relation to clinical severity (more vs. less severe) and mutation groups. Although data on the MECP2 mutation were available, six broad categories were created to avoid subgroups being too small: Missense (n = 23, 25.3%), Early Truncating (n = 26, 28.6%), Late Truncating (n = 7, 7.7%), C-Terminal (n = 13, 14.3%), Large Deletion (n = 2, 2.2%) and No Known Mutation (n = 20, 22.0%). Disregarding the last category, the remaining five categories were then combined into two broader mutation groups: (a) Early Truncating and Large Deletion, and (b) Missense, Late Truncating and C-Terminal, in line with the findings of Neul et al. . Cross tabulation with associated chi-squared tests, non-parametric Mann–Whitney U tests or Kruskal-Wallis analysis of variance with post hoc Mann–Whitney U tests together with non-parametric (Spearman) correlations were used to explore differences between groups and relationships between variables.
Behavioural characteristics of the RTT sample
The percentage occurrence of potentially characteristic behaviour in this RTT sample is also given in Table 1, alongside findings from the five previous surveys mentioned in the introduction. Hand stereotypies were almost universal (99%). Teeth grinding (58%), sleeping difficulties and night-time laughing (64%), anxiety or inappropriate fear (73%), low mood/changeable mood (77%), breath holding (63%) and hyperventilation (77%) were reported among the majority.
RSBQ total and subscale mean scores, SDs, ranges and maximum scores
Total (max = 90)
12 to 78
General mood (max = 16)
0 to 16
Breathing problems (max = 10)
0 to 10
Hand behaviours (max = 12)
1 to 12
Repetitive face movements (max = 8)
0 to 8
Body rocking and expressionless face (max = 12)
1 to 12
Night-time behaviours (max = 6)
0 to 6
Fear/anxiety (max = 8)
0 to 8
Walking/standing (max = 8)
0 to 4
Non-parametric correlation matrix for RSBQ subscale scores
General mood (GM)
Breathing problems (BP)
Hand behaviours (HB)
Repetitive face movements (RP)
Body rocking/expressionless face (BREF)
Night-time behaviours (NT)
Overactivity and impulsivity
Overactivity and impulsivity among the RTT and contrast groups: mean Activity Questionnaire scores (SD, range)
( N = 88)
( N = 66)
14.4 (11.94, 0 to 52)
33.1 (14.92,0 to 60)
8.6 (6.30, 0 to 31)
18.7 (8.92, 0 to 37)
5.8 (7.03, 0 to 24)
14.4 (7.91, 0 to 24)
2.8 (6.0, 0 to 24)
9.8 (7.67, 0 to 24)
8.6 (6.81, 0 to 22)
18.6 (5.48, 6 to 24)
Mood, interest and pleasure
Mood, interest and pleasure among the RTT and contrast groups: mean MIPQ-S scores (SD, range)
( N = 88)
( N = 66)
33.9 (5.76, 19 to 45)
33.7 (7.79, 4 to 47)
19.7 (2.50, 11 to 24)
19.1 (4.19, 0 to 24)
Interest and pleasure
14.2 (4.09, 7 to 24)
14.6 (4.57, 4 to 23)
Repetitive behaviour among the RTT and contrast groups: mean Repetitive Behaviour Questionnaire scores (SD, range)
( N = 88)
( N = 66)
6.9 (4.31,0 to 24)
13.9 (7.67, 3 to 36)
5.5 (2.90, 0 to 12)
8.8 (3.22, 0 to 12)
0.03 (0.31, 0 to 3)
1.5 (2.60, 0 to 12)
Insistence of sameness
0.7 (1.64, 0 to 8)
1.2 (2.09, 0 to 8)
Within the RTT group, there were no significant RBQ total or subscale differences across clinical severity categories or across mutation groups.
Percentage occurrence of self injury topographies among the RTT and contrast group who self-injure
( n = 24)
( n = 18)
Hit self with body part
Hit self against surface
Hit self with object
In this paper, we have presented behavioural data on 91 girls and women with RTT. The behavioural characteristics of all but three who had preserved language were compared to a contrast group with a range of other genetic conditions matched for gender, age, language and daily living skills. The RTT sample was drawn from a national database and was reasonably large for a study of RTT. All families whose children met the criteria were invited to participate. In particular, both children and adults were represented, the latter being the slight majority. However, the sample was skewed towards those living in the family home as an additional research purpose was to investigate the relationship between child characteristics and parental well-being. The 11 participants in out-of-family placements were, on average, older than those living in the family home (mean, 28.0 years vs. 19.5 years), albeit that the two groups were similar in age among the adults: almost all of the children lived with their parents. In addition, the two groups were similar in diagnostic distribution (82% classic vs. 75%), mean age of regression (18.5 months vs. 19.3) and mean severity score (9.0 vs. 8.5).
The response rate was low and it is not possible to assess the representativeness of the achieved sample. However, the age distribution was similar to a recent all-age, large sample (n = 983) study of gastrointestinal and feeding problems . Moreover, over three-quarters of the sample had a positive mutation in the MECP2 gene. Not all individuals in the sample had been tested, but in only one case diagnosed with classic RTT was a MECP2 mutation not found. This is consistent with the literature that a mutation in the MECP2 gene can be found in over 90% of cases with Classic RTT . Consistent with other studies, the most common age of regression was between 12 and 18 months.
A further weakness of the study is that the comparison to the contrast group could only be achieved in relation to measures that had already been administered in relation to the other syndrome groups in studies conducted by the Cerebra Centre. Therefore, this study does not contain comparative data on certain RTT specific issues relevant to a potential RTT behavioural phenotype. Findings in this survey do support previous studies that hand stereotypies were almost universal and that breathing irregularities, night-time unrest, anxiety or inappropriate fear and low or changeable mood were common. However, in general, we cannot comment on their frequency relative to the contrast group.
It is possible to be more definitive about hand stereotypies as comparison of repetitive behaviour between the RTT sample and the contrast group provides further evidence for their characteristic occurrence. Hand stereotypies were the only area found to be more common among the RTT group. In other respects, stereotypic and compulsive behaviour were greater among the contrast group. However, even in relation to hand stereotypies, it should be noted that these were found among over two-thirds of the contrast group and in an equally high proportion to the RTT sample among those in the contrast group with Angelman syndrome (80%). Hence, one could conclude that hand stereotypies are characteristic of people with the degree of intellectual disability found in the two groups in this study, while it may be the particular form of hand stereotypy that is diagnostic of a particular syndrome: such as hand wringing in RTT and hand flapping in Angelman syndrome .
Overactivity and impulsivity were not characteristic of RTT, with scores on both AQ subscales below those found for the contrast group. Moreover, despite low or changeable mood being commonly reported in RTT, the RTT group did not differ from the contrast group with respect to either mood or interest and pleasure. A low, albeit possibly clinically important, proportion of the RTT group was found to have abnormally low mood.
Self-injury was reported only in a minority of the RTT sample and in a lower proportion than in three previous surveys (Table 1). It was also found to be less common when compared to the contrast group. The most frequent category of self-injury reported among the RTT group was rubbing or scratching self. This topography is compatible with their low level of functional hand use. Self-injury in the RTT sample was associated with overactivity and impulsivity, a finding consistent with the predictors of self-injury in certain other syndromes and in autistic spectrum disorders [16,27-29]. Overactivity and impulsivity were in turn associated with mutation group, occurring less among Early Truncating mutations and Large Deletions, which are associated with greater severity of disability. This would suggest that self-injury would occur more among individuals with severity scores in the mild range and this was found to be the case.
The ranges in the RSBQ total and subscale scores found for this RTT sample were wide and indicate that there is variability in the manifestation of the behavioural phenotype across individuals. For example, variability in Hand Behaviours and Repetitive Face Movements subscale scores were related to mutation group, with greater severity being associated with Early Truncating and Large Deletion mutations. However, the strength of positive association between the majority of subscales suggests the tendency for some individuals to have relatively high problem levels in all areas while others will generally have relatively low problem levels.
Mount et al.  and Robertson et al.  report RSBQ means for child samples. Findings for this child and adult sample differ from the Mount et al. survey in certain respects. Scores for the total scale and for the Breathing Abnormalities, Body Rocking and Expressionless Face, Night-time Behaviour and Fear/Anxiety subscales were similar. Subscale scores for General Mood, Repetitive Face Movements and Walking/Standing were significantly lower (respectively t = 3.27, 2.20, 2.33, df = 227, P < .01, .05, .05) while that for Hand Behaviours was significantly higher (t = 2.85, df = 227, P < .01). Where differences existed, the means given in Robertson et al. were closer to those reported here for all subscales other than Repetitive Face Movements.
In conclusion, this study provides further evidence in support of hand stereotypies, breathing irregularities, night-time unrest and anxiety or inappropriate fear being part of a RTT behavioural phenotype, although only the former was tested against its occurrence in a contrast group and, even here, the conclusion may need to be limited to a particular form of hand stereotypy. Problems of low mood were also reported as common. However, mood and interest and pleasure were no lower than found in the contrast group. In addition, self-injury was lower than in the contrast group and was associated with factors found to predict self-injury in other groups of people with severe intellectual disabilities. Moreover, there is variability in the manifestation of problem behaviours potentially associated with the syndrome across individuals, with some more severely affected in most areas than others. Some of this variability appears to be underpinned by genetic mutation.
Ethical approval was provided by the Research Ethics Committee for Wales, Cardiff, Wales, UK.
This project was funded by the NISCHR Social Care Studentship scheme. We would like to thank the families and individuals who agreed to take part and the Rett UK for their support of the study and the BIRSS database.
NISCHR had no involvement in the writing of this paper or the decision to submit the paper for publication.
- Amir RE, Veyver IB, Wan M, Tran CQ, Franckle U, Zoghbi HY. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG – binding protein 2. Nat Genet. 1999;23:185–7.View ArticlePubMedGoogle Scholar
- Hagberg B. Clinical manifestations and stages of Rett syndrome. Ment Retard Dev D R. 2002;8:61–5.View ArticleGoogle Scholar
- Neul JL, Kaufmann W, Glaze DG, Christodoulou J, Clarke AJ, Bahi-Buisson N, et al. Rett syndrome: revised diagnostic criteria and nomenclature. Ann Neurol. 2010;68:944–50.View ArticlePubMed CentralPubMedGoogle Scholar
- Hagberg B, Hanefeld F, Percy A, Skjeldal O. An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett syndrome clinical Criteria Consensus Panel Satellite to European Paediatric Neurology Society Meeting, Baden Baden, Germany, 11 September 2001. Eur Paediatr Neurol. 2002;6:293–7.View ArticleGoogle Scholar
- Mount RH, Hastings RP, Reilly S, Cass H, Charman T. Towards a behavioral phenotype for Rett syndrome. Am J Ment Retard. 2003;108:1–12.View ArticlePubMedGoogle Scholar
- Mount RH, Hastings RP, Reilly S, Cass H, Charman T. Behavioural and emotional features in Rett syndrome. Disabil Rehabil. 2001;23:129–38.View ArticlePubMedGoogle Scholar
- Mount RH, Hastings RP, Reilly S, Cass H, Charman T. Behaviour problems in adult women with Rett syndrome. J Intell Disabil Res. 2002;46:619–24.View ArticleGoogle Scholar
- Coleman M, Brubaker J, Hunter K, Smith G. Rett syndrome: a survey of North American patients. J Ment Def Res. 1988;32:117–24.Google Scholar
- Sansom D, Krishnan V, Corbett J, Kerr A. Emotional and behavioural aspects of Rett syndrome. Dev Med Child Neurol. 1993;35:340–5.View ArticlePubMedGoogle Scholar
- Cass H, Reilly S, Owen L, Wisbeach A, Weekes L, Slonims V, et al. Findings from a multidisciplinary clinical case series of females with Rett syndrome. Dev Med Child Neurol. 2003;45:325–37.View ArticlePubMedGoogle Scholar
- Halbach NS, Smeets EE, Schrander-Stumpel CT, Van Schrojenstein Lantman De Valk HH, Maaskant MA, Curfs LM. Aging in people with specific genetic syndromes: Rett syndrome. Am J Med Genet A. 2008;146A:1925–32.View ArticlePubMedGoogle Scholar
- Arron K, Oliver C, Berg K, Moss J, Burbidge C. Prevalence and phenomenology of self-injurious and aggressive behaviour in genetic syndromes. J Intell Disabil Res. 2011;55:109–20.View ArticleGoogle Scholar
- Ross E, Oliver C. The relationship between levels of mood, interest and pleasure and ‘challenging behaviour’ in adults with severe and profound intellectual disability. J Intell Disabil Res. 2002;46:191–7.View ArticleGoogle Scholar
- Vos P, de Cock P, Petry K, Van Den Noortgate W, Maes B. What makes them feel like they do? Investigating the subjective well-being in people with severe and profound disabilities. Res Dev Disabil. 2010;31:1623–32.View ArticlePubMedGoogle Scholar
- Cianfaglione R, Clarke A, Kerr M, Hastings R, Oliver C, Moss J, et al. A national survey of Rett syndrome1: age, clinical characteristics, current abilities and health. Am J Med Gen. in press.Google Scholar
- Oliver C, Berg K, Moss J, Arron K, Burbidge C. Delineation of behavioural phenotypes in genetic syndromes: Characteristics of autism spectrum disorder, affect and hyperactivity. J Autism Dev Disord. 2011;41:1019–32.View ArticlePubMedGoogle Scholar
- Moss J, Oliver C, Arron K, Burbidge C, Berg K. The prevalence and phenomenology of repetitive behaviour in genetic syndromes. J Autism Dev Disord. 2009;39:572–88.View ArticlePubMedGoogle Scholar
- Smeets EEJ, Chenault M, Curfs LMG, Schrander-Stumpel CTRM, Frijns JP. Rett syndrome and long-term disorder profile. Am J Med Genet A. 2009;149A:199–205.View ArticlePubMedGoogle Scholar
- Mount RH, Charman T, Hastings R, Reilly S, Cass H. The Rett Syndrome Behaviour Questionnaire (RSBQ): refining the behavioural phenotype of Rett syndrome. J Child Psychol Psyc. 2002;43:1099–110.View ArticleGoogle Scholar
- Burbidge C, Oliver C, Moss J, Arron K, Berg K, Furniss F, et al. The association between repetitive behaviours, impulsivity and hyperactivity in people with intellectual disability. J Intell Disabil Res. 2010;54:1078–92.View ArticleGoogle Scholar
- Ross E, Oliver C. Preliminary analysis of the psychometric properties of the Mood, Interest And Pleasure Questionnaire (MIPQ) for adults with severe and profound learning disabilities. Brit J Clin Psychol. 2003;42:81–93.View ArticleGoogle Scholar
- Ross E, Arron K, Oliver C. The mood interest and pleasure questionnaire: manual for administration and scoring. Birmingham, UK: The Cerebra Centre, University of Birmingham; 2008.Google Scholar
- Hyman P, Oliver C, Hall S. Self-injurious behaviour, self restraint and compulsive behaviour in Cornelia de Lange syndrome. Am J Ment Retard. 2002;107:146–54.View ArticlePubMedGoogle Scholar
- Neul JL, Fang P, Barrish J, Lane J, Caeg EB, Smith EO, et al. Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome. Neurology. 2008;70:1313–21.View ArticlePubMed CentralPubMedGoogle Scholar
- Motil KJ, Caeg E, Barrish JO, Geerts SP, Lane JB, Percy AK, et al. Gastrointestinal and nutritional problems occur frequently throughout life in girls and women with Rett syndrome. J Pediatr Gastroenterol Nutr. 2012;55:292–298.19.View ArticlePubMed CentralPubMedGoogle Scholar
- Oliver C, Adams D, Allen D, Bull L, Heald M, Moss J, et al. Causal models of clinically significant behaviors in Angelman, Cornelia de Lange, Prader-Willi and Smith-Magenis syndromes. Int Rev Res Dev Disabil. 2013;44:167–212.View ArticleGoogle Scholar
- Oliver C, Sloneem J, Arron K. Self-injurious behaviour in Cornelia de Lange syndrome: I. Prevalence and phenomenology. J Intell Disabil Res. 2009;53:575–89.View ArticleGoogle Scholar
- Richards C, Oliver C, Nelson L, Moss J. Self-injurious behaviour in individuals with autism spectrum disorder and intellectual disability. J Intell Disabil Res. 2012;56:476–89.View ArticleGoogle Scholar
- Richman DM, Barnard-Brak L, Bosch A, Thompson S, Grubb L, Abby L. Predictors of self-injurious behaviour exhibited by individuals with autism spectrum disorder. J Intell Disabil Res. 2013;57:429–39.View ArticleGoogle Scholar
- Robertson L, Hall SE, Jacoby P, Ellaway C, de Klerk N, Leonard H. The association between behaviour and genotype in Rett Syndrome using the Australian Rett Syndrome Database. Am J Med Genet B Neuropsychiatr Genet. 2006;141B:177–83.View ArticlePubMed CentralPubMedGoogle Scholar
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