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Congenital nystagmus

MONDO:0005712

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)

Also known as: nystagmus, congenital idiopathic nystagmus, congenital pathologic nystagmus, motor congenital nystagmus, nystagmus, congenital

6 clinical trials for this condition and its sub-types.

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Sub-types

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

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Human disease (14) Pathologic nystagmus (6) Hereditary neurological disease (5) Ocular motility disease (4) Cranial nerve neuropathy (3) Disease of genetic or genomic mechanism (2) Congenital nervous system disorder (1)
Trials to join now! 2 Not yet recruiting 2 Completed 2
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