Bilateral anterior segment dysgenesis and persistent fetal vasculature associated with terminal 10q26 deletion

Jessica F. Yang; Ramak Roohipourmoallai; Penny E. Straughn; Mark B. Sherwood; Swati Agarwal-Sinha; Roberto T. Zori; Siva S.R. Iyer

doi:10.1016/j.jaapos.2021.05.014

Bilateral anterior segment dysgenesis and persistent fetal vasculature associated with terminal 10q26 deletion

Jessica F. Yang
, Ramak Roohipourmoallai
, Penny E. Straughn
, Mark B. Sherwood
, Swati Agarwal-Sinha
, Roberto T. Zori
, Siva S.R. Iyer

Department of Ophthalmology and Visual Sciences

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

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.[Formula

Original language	English
Pages (from-to)	309-311
Number of pages	3
Journal	Journal of AAPOS
Volume	25
Issue number	5
DOIs	https://doi.org/10.1016/j.jaapos.2021.05.014
State	Published - Oct 2021

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10.1016/j.jaapos.2021.05.014

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title = "Bilateral anterior segment dysgenesis and persistent fetal vasculature associated with terminal 10q26 deletion",

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.[Formula",

author = "Yang, \{Jessica F.\} and Ramak Roohipourmoallai and Straughn, \{Penny E.\} and Sherwood, \{Mark B.\} and Swati Agarwal-Sinha and Zori, \{Roberto T.\} and Iyer, \{Siva S.R.\}",

note = "Publisher Copyright: {\textcopyright} 2021 American Association for Pediatric Ophthalmology and Strabismus",

year = "2021",

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doi = "10.1016/j.jaapos.2021.05.014",

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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.

PY - 2021/10

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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 - https://www.scopus.com/pages/publications/85119039903

U2 - 10.1016/j.jaapos.2021.05.014

DO - 10.1016/j.jaapos.2021.05.014

M3 - Article

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ER -

Bilateral anterior segment dysgenesis and persistent fetal vasculature associated with terminal 10q26 deletion

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