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A case of unilateral sectoral iris heterochromia in an infant with Beckwith-Wiedemann syndrome
PURPOSE: To report a case of unilateral sectoral iris heterochromia in an infant with Beckwith-Wiedemann syndrome (BWS). OBSERVATIONS: An 8-month-old girl known case of BWS, due to hypomethylation of the DMR2 (KCNQ1OT1) on chromosome 11p15.5, with features of macroglossia, neonatal hypoglycaemia and...
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| Publicado no: | Am J Ophthalmol Case Rep |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8220324/ https://ncbi.nlm.nih.gov/pubmed/34189344 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajoc.2021.101150 |
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