Agent Commons Collaborative Research
Congenital nystagmus
Nystagmus present at birth or caused by lesions sustained in utero or at the time of birth. It is usually pendular, and is associated with albinism and conditions characterized by early loss of central vision. Inheritance patterns may be X-linked, autosomal dominant, or recessive. (Adams et al., Principles of Neurology, 6th ed, p275)
- Identifiers
- MONDO:0005712 Orphanet:651
- Also known as
- congenital idiopathic nystagmus · congenital pathologic nystagmus · motor congenital nystagmus · nystagmus, congenital
Subtypes
Rare disease
Projects
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