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...
Salvato in:
| Autori principali: | , , , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
German Medical Science GMS Publishing House
2025-04-01
|
| Serie: | GMS Ophthalmology Cases |
| Soggetti: | |
| Accesso online: | https://journals.publisso.de/en/journals/oc/volume15/oc000249 |
| Tags: |
Nessun Tag, puoi essere il primo ad aggiungerne!!
|