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Treatment of Life-Threatening Self-Injurious Behavior Secondary to Hereditary Sensory and Autonomic Neuropathy Type II: A Controlled Case Study
David Kuhn, PhD*,
Louis Hagopian, PhD,
and
Cindy Terlonge, BA
Kennedy Krieger Institute, Baltimore, Maryland
* To whom correspondence should be addressed. E-mail: kuhn{at}kennedykrieger.org.
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Abstract |
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Although self-injurious behavior is present in all subtypes of hereditary sensory and autonomic neuropathy, the literature has not sufficiently addressed the issue of treatment of self-injury in this population. Therefore, the purpose of the current case study was to describe a method for assessing and treating self-injurious behavior associated with hereditary sensory and autonomic neuropathies. This study was conducted with an 11-year-old boy diagnosed with hereditary sensory and autonomic neuropathy type II admitted to an inpatient behavioral unit over a 4-month period. A simplified version of a habit reversal treatment was used, consisting of awareness training, self-monitoring, competing responses, and social support. Treatment resulted in a 98% reduction in the rate of self-injurious behavior relative to pretreatment baseline rates. This case study illustrates that behavioral interventions may be a viable option for treating self-injury secondary to hereditary sensory and autonomic neuropathies.
First published on January 9, 2008, doi:10.1177/0883073807309236
Journal of Child Neurology 2008;23:381.
A more recent version of this article appeared on April 1, 2008

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