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Up to: Hereditary neurological disease · Congenital nervous system disorder · Pathologic nystagmus

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)

4 trials tagged with this condition →

Spinocerebellar ataxia 27A 1 trial
Nystagmus 1, congenital, X-linked 0 trials
Nystagmus 2, congenital, autosomal dominant 0 trials
Nystagmus 3, congenital, autosomal dominant 0 trials
Nystagmus 5, congenital, X-linked 0 trials
Nystagmus 6, congenital, X-linked 0 trials
Nystagmus 7, congenital, autosomal dominant 0 trials
Nystagmus, congenital, autosomal recessive 0 trials
Nystagmus, hereditary vertical 0 trials
Nystagmus, myoclonic 0 trials