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Rett syndrome: the bcl-2 gene--a mediator of neurotrophic mechanisms?
M Anvret1, Z P Zhang, B Hagberg
1Department of Clinical Genetics, Karolinska Hospital, Stockholm, Sweden.
Abstract:
Rett syndrome affects young girls. The molecular basis is mysterious. One tenable hypothesis can be that the programmed early infantile death of neuronal cells is reprogrammed. The bcl-2 gene on chromosome 22 has been shown to play a role in the apoptosis process. No sequence abnormalities were detected in the bcl-2 gene of 6 patients with Rett syndrome which could explain the pathophysiology of Rett syndrome.
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