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PMID: 3058791 Published · ppublish English Journal Article Review

Genetic aspects of Rett syndrome.

Journal of child neurology ·Vol. 3 Suppl ·1988-00-00 ·Pages S76-8

Zoghbi H

Abstract

To date over 1,000 cases of Rett syndrome have been described in females exclusively. Some of these cases, less than 2 in 100, are familial. The inheritance through maternal lines in the familial cases suggests that Rett syndrome is an X-linked disorder lethal in males. Hypotheses about the genetic mechanisms involved in this syndrome along with suggestions to approach the molecular basis of this disorder are presented.

MeSH Terms
Ammonia/blood Autistic Disorder/genetics Child Diseases in Twins Female Genetic Linkage Humans Neurocognitive Disorders/genetics Sex Chromosome Aberrations/genetics Syndrome X Chromosome
Chemicals
Ammonia
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Zoghbi H
Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030.
Article Info
Journal
Journal of child neurology
Abbr.
J Child Neurol
ISSN
0883-0738
Published
1988-00-00
Pages
S76-8
Language
English
Region
United States
NLM ID
8606714
Subset
IM
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