motor apraxia

Cogan type ocular motor apraxia is a genetic condition for which the inheritance pattern has not been well established.

Studies of gestural ability incorporating BPO measures consider aspects of cognition, language, language impairment, and motor apraxia.

Studies of motor apraxia use BPO measures to better understand gestural impairment in apraxic patients, and often consider aphasia as an apraxic phenomenon.

Oculomotor apraxia (OMA), also known as Cogan's Ocular Motor Apraxia or Saccadic Initiation Failure (SIF) is the absence or defect of controlled, voluntary, and purposeful eye movement.

Congenital Oculomotor Apraxia oculomotor apraxia, Cogan type COMA saccade initiation failure, congenital None Cogan type ocular motor apraxia is a rare inherited eye disorder that is present at birth (congenital).