TY - JOUR
T1 - Bilateral anterior segment dysgenesis and persistent fetal vasculature associated with terminal 10q26 deletion
AU - Yang, Jessica F.
AU - Roohipourmoallai, Ramak
AU - Straughn, Penny E.
AU - Sherwood, Mark B.
AU - Agarwal-Sinha, Swati
AU - Zori, Roberto T.
AU - Iyer, Siva S.R.
N1 - Publisher Copyright:
© 2021 American Association for Pediatric Ophthalmology and Strabismus
PY - 2021/10
Y1 - 2021/10
N2 - 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.[Formula
AB - 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.[Formula
UR - http://www.scopus.com/inward/record.url?scp=85119039903&partnerID=8YFLogxK
U2 - 10.1016/j.jaapos.2021.05.014
DO - 10.1016/j.jaapos.2021.05.014
M3 - Article
C2 - 34582953
AN - SCOPUS:85119039903
SN - 1091-8531
VL - 25
SP - 309
EP - 311
JO - Journal of AAPOS
JF - Journal of AAPOS
IS - 5
ER -