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J Intellect Disabil Res ; 55(10): 973-87, 2011 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-21790824

RESUMEN

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.


Asunto(s)
Anomalías Múltiples/diagnóstico , Anomalías Múltiples/genética , Trastorno Autístico/diagnóstico , Trastorno Autístico/genética , Enfermedades del Desarrollo Óseo/diagnóstico , Enfermedades del Desarrollo Óseo/genética , Trastornos de la Conducta Infantil/diagnóstico , Trastornos de la Conducta Infantil/genética , Anomalías Craneofaciales/diagnóstico , Anomalías Craneofaciales/genética , Discapacidad Intelectual/diagnóstico , Discapacidad Intelectual/genética , Fenotipo , Displasia Septo-Óptica/diagnóstico , Displasia Septo-Óptica/genética , Anomalías Múltiples/psicología , Adaptación Psicológica , Adolescente , Trastorno Autístico/psicología , Enfermedades del Desarrollo Óseo/psicología , Niño , Trastornos de la Conducta Infantil/psicología , Preescolar , Comunicación , Anomalías Craneofaciales/psicología , Análisis Mutacional de ADN , Discapacidades del Desarrollo/diagnóstico , Discapacidades del Desarrollo/genética , Discapacidades del Desarrollo/psicología , Femenino , Humanos , Discapacidad Intelectual/psicología , Masculino , Factores de Transcripción NFI/genética , Examen Neurológico , Pruebas Neuropsicológicas , Determinación de la Personalidad , Pronóstico , Displasia Septo-Óptica/psicología
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