<i>MECP2</i> Duplication Syndrome
Author(s) -
Hilde Van Esch
Publication year - 2011
Publication title -
molecular syndromology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.609
H-Index - 36
eISSN - 1661-8777
pISSN - 1661-8769
DOI - 10.1159/000329580
Subject(s) - gene duplication , mecp2 , etiology , medicine , intellectual disability , genetics , pediatrics , gene , psychiatry , biology , phenotype
Since the initial report that clearly established a causal role between duplication of the MECP2 gene and a severe syndromic form of intellectual disability, many new patients have been identified and reported, and the etiology in already published families solved. This has led to the establishment of a clinically recognizable disorder. Here, we review the clinical data of 129 reported and nonreported male patients with MECP2 duplication syndrome.
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