MeSH Browser

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 MeSH Supplementary Concept Data 2025