| ocular a., autosomal recessive |
a severe form of OA in which both males and females are as severely affected as are hemizygous males with X-linked OA.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| ocular a., Forsius-Eriksson type |
Forsius-Eriksson syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| ocular a., Nettleship-Falls type |
X-linked (Nettleship) (XOAN) ocular albinism.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| ocular a., X-linked (Nettleship) |
the classic type of OA; hemizygous males are affected with reduced pigmentation of the irides, nystagmus, head nodding and tilting, photophobia, decreased visual acuity of varying degree, and strabismus; the pupillary reflex is present; the fundus is depigmented; and the choroidal vessels stand out. Heterozygous females show translucent irides and a mosaic of pigmentation in the fundus due to lyonization and may also show nystagmus and photophobia. Called also OA1 and Nettleship-Falls type ocular a.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| ocular b. |
a jerky downward deviation of the eyes with slow return to the middle position, seen in comatose patients and thought to be due to a pontine lesion.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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