ArticleGMS ophthalmology cases2017
A case of morning glory syndrome associated with persistent hyperplastic primary vitreous and Peters' anomaly.
Article in GMS ophthalmology cases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
4 citing papers in PubMed, 7 citations in OpenAlex.
- Progress in the Management of Retinal Detachment Associated With Morning Glory Syndrome.Clinical ophthalmology (Auckland, N.Z.) · 2025Review
- Outcomes and surgical management of persistent fetal vasculature.BMJ open ophthalmology · 2021Article
- Bilateral primary hyperplastic persistent vitreous: report of two cases.GMS ophthalmology cases · 2020Article
- Pediatric cataract surgery in congenital anterior segment dysmorphology: An overview.Taiwan journal of ophthalmologyReview
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We report a case of morning glory syndrome (MGS) associated with persistent hyperplastic primary vitreous (PHPV) and Peters' anomaly. A 2-day-old girl, born at term with a birth weight of 3,350 g was diagnosed with Peters' anomaly, cataract, microphthalmia, PHPV, and MGS. A right limbal lensectomy and vitrectomy with stalk cauterization was performed 8 days later. No early postoperative complication occurred, the family was discharged with advice on medication, and follow-up examination was scheduled. The case report reveals the coexistence of PHPV, Peters' anomaly, and MGS, which may suggest a genetic link.
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Registered trials
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