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Rett syndrome: case reports and management strategies.

Rett Syndrome (RS) is a mental retardation syndrome occurring in females consisting of normal pre-, peri-, and neonatal growth and development, followed by rapid regression after 3 but before 30 months, an arrest of the regression and a developmental plateau. The regression results in autistic behavior, with loss of production and comprehension of language, seizures, hyperventilation, characteristic hand-wringing, and ataxic gait. Four case histories of RS from the authors' practice are presented. Management strategies are presented and needed research is suggested.[1]

References

  1. Rett syndrome: case reports and management strategies. Burd, L., Gascon, G., Kerbeshian, J. Neuroscience and biobehavioral reviews. (1988) [Pubmed]
 
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