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. 1995 Jul;73(1):77–81. doi: 10.1136/adc.73.1.77

Behaviour in mucopolysaccharide disorders.

M C Bax 1, G A Colville 1
PMCID: PMC1511159  PMID: 7639557

Abstract

This paper reports a study of the nature and prevalence of behaviour problems in 258 children with mucopolysaccharide disorders. Questionnaire data obtained through the post was supplemented by home visits to 42 families in the sample and by regular discussions with families at meetings of the Society for Mucopolysaccharide Diseases. High rates of behaviour problems were found, particularly in children with Sanfilippo's and Hunter's disease aged 5 to 9 years. These included destructiveness, restlessness, and aggressiveness. Sleep problems were common across subtypes with an overall prevalence of 66%. Parents reported that they received little or no support in the management of these difficult behaviours. It is concluded that behaviour problems are a primary feature of the mucopolysaccharide disorders and place a major strain on families. Services to help families cope with these problems are urgently needed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Christie R., Bay C., Kaufman I. A., Bakay B., Borden M., Nyhan W. L. Lesch-Nyhan disease: clinical experience with nineteen patients. Dev Med Child Neurol. 1982 Jun;24(3):293–306. doi: 10.1111/j.1469-8749.1982.tb13621.x. [DOI] [PubMed] [Google Scholar]
  2. Clements J., Wing L., Dunn G. Sleep problems in handicapped children: a preliminary study. J Child Psychol Psychiatry. 1986 May;27(3):399–407. doi: 10.1111/j.1469-7610.1986.tb01841.x. [DOI] [PubMed] [Google Scholar]
  3. Curfs L. M., Verhulst F. C., Fryns J. P. Behavioral and emotional problems in youngsters with Prader-Willi syndrome. Genet Couns. 1991;2(1):33–41. [PubMed] [Google Scholar]
  4. Greenswag L. R. Adults with Prader-Willi syndrome: a survey of 232 cases. Dev Med Child Neurol. 1987 Apr;29(2):145–152. doi: 10.1111/j.1469-8749.1987.tb02129.x. [DOI] [PubMed] [Google Scholar]
  5. Nidiffer F. D., Kelly T. E. Developmental and degenerative patterns associated with cognitive, behavioural and motor difficulties in the Sanfilippo syndrome: an epidemiological study. J Ment Defic Res. 1983 Sep;27(Pt 3):185–203. doi: 10.1111/j.1365-2788.1983.tb00291.x. [DOI] [PubMed] [Google Scholar]
  6. Richman N., Stevenson J. E., Graham P. J. Prevalence of behaviour problems in 3-year-old children: an epidemiological study in a London borough. J Child Psychol Psychiatry. 1975 Oct;16(4):277–287. doi: 10.1111/j.1469-7610.1975.tb00362.x. [DOI] [PubMed] [Google Scholar]
  7. Turk J. The fragile-X syndrome. On the way to a behavioural phenotype. Br J Psychiatry. 1992 Jan;160:24–35. doi: 10.1192/bjp.160.1.24. [DOI] [PubMed] [Google Scholar]
  8. van de Kamp J. J., Niermeijer M. F., von Figura K., Giesberts M. A. Genetic heterogeneity and clinical variability in the Sanfilippo syndrome (types A, B, and C). Clin Genet. 1981 Aug;20(2):152–160. doi: 10.1111/j.1399-0004.1981.tb01821.x. [DOI] [PubMed] [Google Scholar]

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