Narbona J
Unidad de Neurología Pediátrica, Clínica Universitaria de Navarra, Facultad de Medicina, Universidad de Navarra, Pamplona, España.
Rev Neurol. 1999;28(1):97-101.
In the last few years, Rett syndrome is conceived as a peculiar form of neurodevelopmental post-migrational disorder affecting dendritogenesis. In this article the clinical pathochronic pattern of classical forms is reviewed and the recent neurobiological and genetic evidences suggesting possible future explanations of its nature and origin are discussed.
在过去几年中，雷特综合征被认为是一种影响树突发生的神经发育迁移后障碍的特殊形式。本文回顾了经典形式的临床病理时间模式，并讨论了最近的神经生物学和遗传学证据，这些证据为其性质和起源提供了可能的未来解释。
