Human genes for Rett syndrome
Rett syndrome [DOID:1206]
A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability.
Synonyms: Rett syndrome, DOID:1206, Rett disease, Rett disorder, Rett syndromes ...