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Cogan type oculomotor Apraxia

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
Also Known As:
Apraxia, oculomotor, Cogan type; Cogan's syndrome, type 2; Congenital Oculomotor Apraxia; Ocular Motor Apraxia; Oculomotor Apraxia, Cogan Type; Saccade initiation failure, congenital
Networked: 12 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Related Diseases

1. Cogan Syndrome
2. Parkinsonian Disorders (Parkinsonism)
3. Myopia
4. Muscular Diseases (Myopathy)
5. Hydrocephalus (Hydrocephaly)

Experts

1. Agarwal, Komal: 1 article (01/2022)
2. Parameswarappa, Deepika C: 1 article (01/2022)
3. Sheth, Jenil: 1 article (01/2022)
4. Liao, Yaping Joyce: 1 article (09/2021)
5. Likitgorn, Techawit: 1 article (09/2021)
6. Yan, Yan: 1 article (09/2021)
7. Bang, Genie M: 1 article (08/2014)
8. Brodsky, Michael C: 1 article (08/2014)
9. Ghadban, Rafif: 1 article (08/2014)
10. Klaehn, Lindsay D: 1 article (08/2014)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Cogan type oculomotor Apraxia:
1. Retinaldehyde (Retinal)IBA
2. Coenzyme A (CoA)IBA
3. Pyruvate CarboxylaseIBA
4. NADH DehydrogenaseIBA
5. Dihydroxyphenylalanine (Dopa)IBA
6. Carbamazepine (Tegretol)FDA LinkGeneric
7. alpha-Fetoproteins (alpha-Fetoprotein)IBA
8. Congenital disorder of glycosylation type 1AIBA
9. A 7 (A-7)IBA