This item still needs to be validated !
ITEM METADATA RECORD
Title: Rett syndrome in females with CTS hot spot deletions: a disorder profile
Authors: Smeets, Eric ×
Terhal, P
Casaer, Paul
Peters, A
Midro, A
Schollen, E
van Roozendaal, K
Moog, U
Matthijs, Gert
Herbergs, J
Smeets, H
Curfs, L
Schrander-Stumpel, C
Fryns, Jean-Pierre #
Issue Date: Dec-2004
Series Title: American Journal of Medical Genetics A vol:132 issue:2 pages:117-20
Abstract: From a series of 107 females with Rett syndrome (RTT), we describe the long-term history of ten females with a deletion in the C-terminus of the MECP2 gene. We observed that their disorder profile is clinically recognizable with time and different from other atypical and milder RTT phenotypes. In females with hot spot deletions in the C-terminus, dystonia is present from childhood and results in a serious spine deformation in spite of preventive measures. Their adaptive behavior is surprisingly better preserved and in contrast with the typical decline in motor functioning. The delineation of disorder profiles by long-term clinical observation can teach us about genotype/phenotype relationships and eventually about the effect of epigenetic phenomena on the final phenotype.
URI: 
ISSN: 1552-4825
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Clinical Genetics Section (-)
Section Child - Miscellaneous (-)
Department of Human Genetics - miscellaneous
× corresponding author
# (joint) last author

Files in This Item:

There are no files associated with this item.

Request a copy

 




All items in Lirias are protected by copyright, with all rights reserved.

© Web of science