Cogan's oculomotor apraxia

GPTKB entity

Statements (18)
Predicate Object
gptkbp:instanceOf gptkb:disease
neurological disorder
gptkbp:affects children
eye movement
gptkbp:firstDescribed gptkb:David_G._Cogan
1952
https://www.w3.org/2000/01/rdf-schema#label Cogan's oculomotor apraxia
gptkbp:ICD-10_code H51.8
gptkbp:inheritance autosomal recessive
gptkbp:OMIM 257550
gptkbp:prevalence rare
gptkbp:symptom head thrusts to compensate for eye movement
delayed saccades
difficulty initiating horizontal eye movements
gptkbp:synonym congenital oculomotor apraxia
gptkbp:treatment supportive therapy
gptkbp:bfsParent gptkb:oculomotor_apraxia
gptkbp:bfsLayer 7