AOA3

Ataxias with oculomotor apraxias (AOAs)

Recommended panel testing at Breda Genetics for this condition: Ataxia-oculomotor apraxia (APTX, PIK3R5, SETX, PNKP) INVOLVING EYE MOVEMENTS Idiopatic oculomotor apraxia Oculomotor apraxia (OMA)  is the absence of,  or a defect in,  the control of voluntary purposeful eye movement.  Children with this condition have difficulty moving their eyes horizontally. Because of this, most patients  with

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