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Behavioural Phenotype of Cornelia De Lange Syndrome

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Journal Arch Dis Child
Specialty Pediatrics
Date 1999 Sep 18
PMID 10490439
Citations 29
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Abstract

A postal questionnaire was used to study 49 individuals with Cornelia de Lange syndrome (including both the classical and the mild forms) to ascertain behavioural phenotype. Ages ranged from early childhood to adulthood (mean age, 10.2 years; SD, 7.8) and the degree of mental retardation from borderline (10%), through mild (8%), moderate (18%), and severe (20%) to profound (43%). A wide variety of symptoms occurred frequently, notably hyperactivity (40%), self injury (44%), daily aggression (49%), and sleep disturbance (55%). These correlated closely with the presence of an autistic like syndrome and with the degree of mental retardation. The frequency and severity of disturbance, continuing beyond childhood, is important when planning the amount and duration of support required by parents.

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References
1.
SHEAR C, Nyhan W, KIRMAN B, Stern J . Self-mutilative behavior as a feature of the de Lange syndrome. J Pediatr. 1971; 78(3):506-9. DOI: 10.1016/s0022-3476(71)80236-6. View

2.
STENGEL E, OLDHAM A, EHRENBERG A . Reactions of low-grade mental defectives to pain. J Ment Sci. 1958; 104(435):434-8. DOI: 10.1192/bjp.104.435.434. View

3.
JOHNSON H, Ekman P, Friesen W . A behavioral phenotype in the de Lange syndrome. Pediatr Res. 1976; 10(10):843-50. DOI: 10.1203/00006450-197610000-00006. View

4.
Wing L, Gould J . Severe impairments of social interaction and associated abnormalities in children: epidemiology and classification. J Autism Dev Disord. 1979; 9(1):11-29. DOI: 10.1007/BF01531288. View

5.
Gillberg C, Terenius L, Lonnerholm G . Endorphin activity in childhood psychosis. Spinal fluid levels in 24 cases. Arch Gen Psychiatry. 1985; 42(8):780-3. DOI: 10.1001/archpsyc.1985.01790310042005. View