FAQ

Oculomotor apraxia

Known as: Ocular motor apraxia, Oculomotor dyspraxia 
Ocular motor apraxia is a deficiency in voluntary, horizontal, lateral, fast eye movements (saccades) with retention of slow pursuit movements. The… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1956-2017
012319562016

Related topics

Related topics

18 relations
ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIAATAXIA-OCULOMOTOR APRAXIA 3ATAXIA-OCULOMOTOR APRAXIA 4ATAXIA-TELANGIECTASIA-LIKE DISORDER 1
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Related mentions per year

Related mentions per year

1953-2018
1960198020002020
Oculomotor apraxia
ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
Oculovestibuloauditory syndrome
Familial aplasia of the vermis
Spinocerebellar Ataxia Type 2
Cardio-facio-cutaneous syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Oculomotor apraxia and dilated cardiomyopathy with ataxia syndrome: A case report.
Dilated cardiomyopathy with ataxia syndrome (DCMA) is a rare mitochondrial condition associated with early onset cardiomyopathy… (More)
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2015
2015
Oculomotor apraxia in Gaucher disease.
A 22-month-old boy born to consanguineous parents presented with mild motor delay and abnormal “thrusting” of head since age 8… (More)
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2013
2013
Saccades and Eye–Head Coordination in Ataxia with Oculomotor Apraxia Type 2
Ataxia with oculomotor apraxia type 2 (AOA2) is one of the most frequent autosomal recessive cerebellar ataxias. Oculomotor… (More)
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2008
2008
Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in 4 families.
BACKGROUND Ataxia with oculomotor apraxia type 2 (AOA2) is an autosomal recessive disease caused by SETX mutations in 9q34… (More)
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2004
2004
Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients.
Ataxia with oculomotor apraxia type 2 (AOA2) is a newly described autosomal recessive cerebellar ataxia (ARCA) defined by genetic… (More)
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2002
2002
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations.
BACKGROUND Early-onset ataxia with hypoalbuminemia is regarded as a variant form of Friedreich ataxia in Japan. Early-onset… (More)
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1996
1996
Intermittent horizontal saccade failure ('ocular motor apraxia') in children.
BACKGROUND Ocular motor apraxia (OMA) in childhood is a poorly understood condition involving a failure of horizontal saccades… (More)
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1995
1995
Neuroradiological and eye movement correlates in children with intermittent saccade failure: "ocular motor apraxia".
Ocular motor apraxia (OMA) is a clinical sign involving the intermittent inability to initiate saccades, and a failure of quick… (More)
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1989
1989
Oculomotor apraxia: the presenting sign of Gaucher disease.
Oculomotor apraxia may be idiopathic or a symptom of a variety of diseases. In Gaucher disease, oculomotor deficit is… (More)
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1987
1987
Ocular motor apraxia associated with intracranial lipoma.
Congenital ocular motor apraxia is rarely associated with brain tumors. A 10-month-old girl with normal vertical eye movements… (More)
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