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Rett syndromeDISORDER

A pervasive developmental disease that is a neurological and developmental disorder that mostly occurs in females and is caused_by a mutation on the MECP2 gene on the X chromosome. Infants with Rett syndrome seem to grow and develop normally at first, but then stop developing and even lose skills and abilities.

Classified under pervasive developmental disorder
Synonyms: cerebroatrophic hyperammonemia
Contributed by: DOntology about three years ago
TASKS associated with Rett syndrome
and their CONTRASTS
No associations have been added.




RELATIONSHIPS to other disorders
 
RETT SYNDROME
 
No child relationships found for this disorder.

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