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Congenital achiasma

ORPHA:324353· ICD-10 H47.4

Definition

Congenital achiasma is a rare, genetic, non-syndromic cranial nerve and nuclear aplasia malformation characterized by the congenital absence of the optic chiasm, resulting from the failure of the optic nerve fibers to cross over and decussate to the contralateral hemisphere, leading to decreased vision, strabismus and congenital nystagmus in infancy.

Prevalence
Unknown
Age of onset
Infancy, Neonatal