Rett Syndrome: Long-Term Clinical Follow-Up Experiences Over Four Decades-Reference-Cited by-同舟云学术

Rett Syndrome: Long-Term Clinical Follow-Up Experiences Over Four Decades

Published:2005-09 Issue:9 Volume:20 Page:722-727
ISSN:0883-0738
Container-title:Journal of Child Neurology
language:en
Short-container-title:J Child Neurol

Author:

Hagberg Bengt¹

Affiliation:

1. Queen Silvia Children's Hospital, Department of Child Neurology, Göteborg University, Göteborg, Sweden, .

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. ( J Child Neurol 2005;20:722—727).

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/08830738050200090401

Reference19 articles.

1. Clinical manifestations and stages of rett syndrome

2. An update on clinically applicable diagnostic criteria in Rett syndrome

3. Rett syndrome: Clinical peculiarities, diagnostic approach, and possible cause

4. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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