X-linked intellectual disability, Cantagrel type
Engelsk navn: X-linked intellectual disability, Cantagrel type
A rare X-linked intellectual disability characterized by marked neonatal hypotonia, progressive quadriparesia, severely delayed developmental milestones (walking at 3 years of age), gastroesophageal reflux, stereotypic movements of the hands, esotropia and infantile autism.
Informasjon
Frambu kompetansesenter for sjeldne diagnoser har kunnskap om diagnosen.
ORPHA: 85277
Klassifiseringsnivå: DisorderICD-10: Q87.8