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Herrenschwand heterochromia
Heterochromatosis
Heterochromia
Heterochromia iridis
Iridal heterochromia
Iridizing

Traduction de «Iridal heterochromia » (Anglais → Français) :



heterochromia iridis [ heterochromatosis | heterochromia ]

hétérochromie [ hétérochromie irienne ]


A rare genetic ocular disease with characteristics of congenital nystagmus (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus an

syndrome d'hypoplasie fovéale-cataracte présénile


A rare X-linked inherited type of ocular albinism described in one African kindred (7 males over 3 generations) to date with characteristics of severe visual impairment, translucent pale-blue irides, a reduction in the retinal pigment and moderately

albinisme oculaire avec surdité sensorielle tardive


heterochromia

hétérochromie irienne | allophtalmie | hétérochromie | hétérophtalmie | yeux vairons






Herrenschwand heterochromia

hétérochromie de Herrenschwand


Canities Greyness, hair (premature) Heterochromia of hair Poliosis:NOS | circumscripta, acquired

Canitie Cheveux gris (prématurément) Hétérochromie des cheveux Poliose:SAI | circonscrite, acquise


A type of oculocutaneous albinism recently discovered in one Chinese family, with characteristics of light hair at birth that darkens with age, white skin, transparent irides, photophobia, nystagmus, foveal hypoplasia and reduced visual acuity. Cause

albinisme oculo-cutané type 6




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Date index: 2024-10-04
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