Development and behaviour in Marshall-Smith syndrome: an exploratory study of cognition, phenotype and autism
- PMID: 21790824
- DOI: 10.1111/j.1365-2788.2011.01451.x
Development and behaviour in Marshall-Smith syndrome: an exploratory study of cognition, phenotype and autism
Abstract
Background: Marshall-Smith syndrome (MSS) is an infrequently described entity characterised by failure to thrive, developmental delay, abnormal bone maturation and a characteristic face. In studying the physical features of a group of patients, we noticed unusual behavioural traits. This urged us to study cognition, behavioural phenotype and autism in six patients.
Methods: Information on development, behavioural characteristics, autism symptoms, and adaptive and psychological functioning of six MSS children was collected through in-person examinations, questionnaires, semi-structured interviews of parents and neuropsychological assessments.
Results: Participants showed moderate to severe delays in mental age, motor development and adaptive functioning, with several similarities in communication, social interactions and behaviour. There was severe delay of speech and motor milestones, a friendly or happy demeanour and enjoyment of social interactions with familiar others. They exhibited minimal maladaptive behaviours. Deficits in communication and social interactions, lack of reciprocal social communication skills, limited imaginary play and the occurrence of stereotyped, repetitive behaviours were noted during assessments.
Conclusions: Systematic collection of developmental and behavioural data in very rare entities such as MSS allows recognition of specific patterns in these qualities. Clinical recognition of physical,developmental and behavioural features is important not only for diagnosis, prognosis and counselling of families, but also increases our understanding of the biological basis of the human physical and behavioural phenotype.
© 2011 The Authors. Journal of Intellectual Disability Research © 2011 Blackwell Publishing Ltd.
Similar articles
-
Development, cognition, and behaviour in Pitt-Hopkins syndrome.Dev Med Child Neurol. 2012 Oct;54(10):925-31. doi: 10.1111/j.1469-8749.2012.04339.x. Epub 2012 Jun 19. Dev Med Child Neurol. 2012. PMID: 22712893 Review.
-
Deletions in the 3' part of the NFIX gene including a recurrent Alu-mediated deletion of exon 6 and 7 account for previously unexplained cases of Marshall-Smith syndrome.Hum Mutat. 2014 Sep;35(9):1092-100. doi: 10.1002/humu.22603. Epub 2014 Jul 8. Hum Mutat. 2014. PMID: 24924640
-
Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhood.Genet Couns. 2012;23(2):135-48. Genet Couns. 2012. PMID: 22876571
-
Malan syndrome: Extension of genotype and phenotype spectrum.Am J Med Genet A. 2018 Dec;176(12):2896-2900. doi: 10.1002/ajmg.a.40663. Epub 2018 Dec 10. Am J Med Genet A. 2018. PMID: 30548146
-
[Chromosome 22q11 deletion syndrome and its relevance for child and adolescent psychiatry. An overview of etiology, physical symptoms, aspects of child development and psychiatric disorders].Z Kinder Jugendpsychiatr Psychother. 2004 May;32(2):107-15. doi: 10.1024/1422-4917.32.2.107. Z Kinder Jugendpsychiatr Psychother. 2004. PMID: 15181786 Review. German.
Cited by
-
Management of an older Marshall-Smith syndrome patient: a review of literature of MSS and craniosynostosis.Childs Nerv Syst. 2024 Aug;40(8):2609-2614. doi: 10.1007/s00381-024-06415-7. Epub 2024 Apr 22. Childs Nerv Syst. 2024. PMID: 38647663 Review.
-
A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith Syndrome.JBMR Plus. 2023 Mar 30;7(6):e10739. doi: 10.1002/jbm4.10739. eCollection 2023 Jun. JBMR Plus. 2023. PMID: 37283649 Free PMC article.
-
Identification of cellular retinoic acid binding protein 2 (CRABP2) as downstream target of nuclear factor I/X (NFIX): implications for skeletal dysplasia syndromes.JBMR Plus. 2024 May 15;8(7):ziae060. doi: 10.1093/jbmrpl/ziae060. eCollection 2024 Jul. JBMR Plus. 2024. PMID: 38827116 Free PMC article.
-
Development, behaviour and sensory processing in Marshall-Smith syndrome and Malan syndrome: phenotype comparison in two related syndromes.J Intellect Disabil Res. 2020 Dec;64(12):956-969. doi: 10.1111/jir.12787. Epub 2020 Oct 9. J Intellect Disabil Res. 2020. PMID: 33034087 Free PMC article.
-
Heterozygosity for nuclear factor one x affects hippocampal-dependent behaviour in mice.PLoS One. 2013 Jun 11;8(6):e65478. doi: 10.1371/journal.pone.0065478. Print 2013. PLoS One. 2013. PMID: 23776487 Free PMC article.
Publication types
MeSH terms
Substances
Supplementary concepts
LinkOut - more resources
Full Text Sources
Medical