Typical presentation of autosomal recessive oculocutaneous albinism in two siblings
Objective: We report the case history and clinical findings in two siblings, a 13-year-old male and a 10-year-old female, who presented with complaints of poor vision since childhood. Both children had blonde hair and depigmented skin. Methods: Ocular examination revealed white eyebrows, white eyel...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
German Medical Science GMS Publishing House
2025-04-01
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| Cyfres: | GMS Ophthalmology Cases |
| Pynciau: | |
| Mynediad Ar-lein: | https://journals.publisso.de/en/journals/oc/volume15/oc000249 |
| Tagiau: |
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
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