X-linked intellectual disability-hypotonia-movement disorder syndrome

A rare, genetic, syndromic intellectual disability characterized by mild to severe intellectual disability associated with variable features, including hypotonia, dyskinesia, spasticity, wide-based gait, microcephaly, epilepsy and behavioral problems. MRI imaging may show a corpus callosum hypoplasia or ventricular enlargement. Other variable features, such as joint hyperlaxity, skin pigmentary abnormalities, and visual impairment, have also been reported.

ORPHA: 457260
Klassifiseringsnivå: Disorder
ICD-10: F78.8

Les mer om X-linked intellectual disability-hypotonia-movement disorder syndrome på orpha.net

Frambu kompetansesenter for sjeldne diagnoser har kunnskap om diagnosen.
Søk på X-linked intellectual disability-hypotonia-movement disorder syndrome på helsebiblioteket.no