| oculocerebrorenal d. |
see under syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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|---|---|
| oculocerebrorenal s. |
an X-linked disorder characterized by vitamin D–refractory rickets, hydrophthalmia, congenital glaucoma and cataracts, mental retardation, and tubule reabsorption dysfunction as evidenced by hypophosphatemia, acidosis, and aminoaciduria. Called also Lowe disease and Lowe-Terrey-MacLachlan s.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| oculocutaneous |
pertaining to or affecting both the eyes and the skin.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| oculocutaneous a. |
a human albinism occurring in ten types all distinguished in their incidence and genetic, biochemical, and clinical characteristics but having in common varying degrees of decreased melanotic pigment of the skin, hair, and eyes, hypoplastic foveas, photophobia, nystagmus, and decreased visual acuity.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| oculocutaneous m. |
see nevus of Ota, under nevus.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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