Zespół Retta.pdf

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Rett syndrome
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Rett syndrome (RTT) is a progressive neurodevelopmental disorder almost exclusively
affecting females. With an incidence of about 1 in 10,000 births, it is a common cause of
profound mental impairment in girls. Typically, babies with RTT develop normally until the
age of 6 to 18 months, when their developmental milestones regress. They lose purposeful use
of their hands and are seriously disabled for life, with reduced muscle tone and seizures. A
temporary "autistic-like" phase often occurs at the onset of the disorder, and older children are
known for their social engagement through intense eye gaze.
RTT is caused by mutations in the gene MeCP2, found on the X chromosome. MeCP2 is called
a "transcriptional repressor" because it codes for a protein that controls the expression of other
genes. Depending on what part of the gene contains the mutation, partial loss of this protein
changes the environment experienced by developmentally important proteins which, in turn,
leads to the RTT phenotype.
MeCP2 mutations seem to be more common in the X chromosome from sperm cells, which
may explain why RTT is rare in boys, who do not inherit an X chromosome from their father.
Girls, however, inherit one copy of the X chromosome from each parent. Girls with RTT have
one functional copy of MeCP2 to counteract the mutated MeCP2 copy. But, in a normal process
called X inactivation, one X chromosome is randomly inactivated in every cell. This results in
the normal copy of MeCP2 being inactivated in some cells but not in others. X-inactivation
coupled with the specific MeCP2 mutation type causes the range of symptoms seen in RTT.
By studying the relationships between the MeCP2 proteins and the proteins affected by it,
investigators hope to develop treatments for Rett syndrome.
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Gene sequence
Genome view see gene locations
Entrez Gene collection of gene-related information
BLink related sequences in different organisms
The literature
Research articles online full text
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Books online books section
OMIM catalog of human genes and disorders
GeneReviews a medical genetics resource
Websites
Information Sheet from the National Institute of Neurological Disorders and Stroke, NIH
International Rett Syndrome Association support and information for families
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Rett syndrome
 

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