Rett syndrome: long-term clinical follow-up experiences over four decades - PubMed (original) (raw)
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Rett syndrome: long-term clinical follow-up experiences over four decades
Bengt Hagberg. J Child Neurol. 2005 Sep.
Abstract
Long-term clinical profiles of female patients with classic Rett syndrome are presented and exemplified by three cases, as experienced over four decades. Emphasized is the frequently surprisingly well-preserved eye contact and primitive memory, in contrast to a premature neuromuscular aging and often advanced peripheral atrophy, usually combined with dystonic-rigid signs that are predominantly right sided.
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