Congenital ocular motor apraxia with autosomal dominant inheritance

American Journal of Ophthalmology

Volumn 129, Issue 6, 2000, Pages 820-822

  Phillips, Paul H ^a   Brodsky, Michael C ^a,b   Henry, Paul M ^a  

^a UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

^b UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; APRAXIA; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRAIN; CASE REPORT; CHILD; CONGENITAL DISORDER; FAMILY; FATHER; FEMALE; HEAD MOVEMENT; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; OPHTHALMOPLEGIA; PRIORITY JOURNAL;

ADULT; APRAXIAS; CHILD; CHILD, PRESCHOOL; EYE DISEASES, HEREDITARY; FEMALE; HUMANS; MALE; OCULAR MOTILITY DISORDERS; PEDIGREE; SACCADES;

EID: 0033854079     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(00)00373-1     Document Type: Article

References (6)

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2. Prasad P., Nair S. Congenital ocular motor apraxia sporadic and familial; support for natural resolution . J Neuro-Ophthalmol. 14:1994;102-104.
3. Gurer Y.K.Y., Kukner S., Kunak B., Yilmaz S. Congenital ocular motor apraxia in two siblings. Pediatr Neurol. 13:1995;261-262.
4. Cogan D.G. Heredity of congenital ocular motor apraxia. Trans Am Acad Ophthalmol Otolaryngol. 76:1972;60-63.
5. Vassella F., Lutschg J., Mumenthaler M. Cogan's congenital ocular motor apraxia in two successive generations. Dev Med Child Neurol. 14:1972;788-803.
6. Borchert M.S., Sadun A.A., Sommers J.D., Wright K.W. Congenital ocular motor apraxia in twins findings with magnetic resonance imaging . J Clin Neuro-ophthalmol. 7:1987;104-107.