Bilateral anterior segment dysgenesis and persistent fetal vasculature associated with terminal 10q26 deletion.
J AAPOS
; 25(5): 309-311, 2021 10.
Article
en En
| MEDLINE
| ID: mdl-34582953
ABSTRACT
Deletion of the 26q position on chromosome 10 results in a syndrome with well-documented systemic phenotypes. There are few reports of ophthalmic manifestations in terminal 10q26 deletion. We report a 4-week-old boy with terminal 10q26 deletion who had extensive ophthalmic abnormalities, including bilateral anterior segment dysgenesis and bilateral persistent fetal vasculature, with microphthalmia, microcornea, iris corectopia, congenital cataracts, and posterior embryotoxon.
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Catarata
/
Anomalías del Ojo
/
Microftalmía
/
Vítreo Primario Hiperplásico Persistente
Tipo de estudio:
Diagnostic_studies
/
Risk_factors_studies
Límite:
Humans
/
Male
Idioma:
En
Año:
2021
Tipo del documento:
Article