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Apraxia, oculomotor, Cogan type MeSH Supplementary Concept Data 2025


MeSH Supplementary
Apraxia, oculomotor, Cogan type
Unique ID
C537423
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C537423
Entry Term(s)
Cogan's syndrome, type 2
Congenital Oculomotor Apraxia
Ocular Motor Apraxia
Oculomotor Apraxia, Cogan Type
Saccade initiation failure, congenital
Registry Numbers
0
Heading Mapped to
Apraxias / congenital
*Cogan Syndrome
Frequency
96
Note
A very rare hereditary condition characterized by defective or absent voluntary horizontal EYE MOVEMENTS and defective or absent horizontal ocular attraction movements. Sympotms usually improve by the first or second decade of life. Inheritance may be autosomal recessive or dominant and variations have been mapped to chromosome 2. OMIM: 257550
Date of Entry
2010/08/25
Revision Date
2016/07/07
Apraxia, oculomotor, Cogan type Preferred
Ocular Motor Apraxia Broader
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