A case of morning glory syndrome associated with persistent hyperplastic primary vitreous and Peters’ anomaly

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 a...

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Autores principales: Muslubas, Isil Sayman, Hocaoglu, Mumin, Arf, Serra, Karacorlu, Murat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: German Medical Science GMS Publishing House 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244077/
https://www.ncbi.nlm.nih.gov/pubmed/28154792
http://dx.doi.org/10.3205/oc000053
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author Muslubas, Isil Sayman
Hocaoglu, Mumin
Arf, Serra
Karacorlu, Murat
author_facet Muslubas, Isil Sayman
Hocaoglu, Mumin
Arf, Serra
Karacorlu, Murat
author_sort Muslubas, Isil Sayman
collection PubMed
description 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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spelling pubmed-52440772017-02-02 A case of morning glory syndrome associated with persistent hyperplastic primary vitreous and Peters’ anomaly Muslubas, Isil Sayman Hocaoglu, Mumin Arf, Serra Karacorlu, Murat GMS Ophthalmol Cases Article 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. German Medical Science GMS Publishing House 2017-01-17 /pmc/articles/PMC5244077/ /pubmed/28154792 http://dx.doi.org/10.3205/oc000053 Text en Copyright © 2017 Muslubas et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License. See license information at http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Muslubas, Isil Sayman
Hocaoglu, Mumin
Arf, Serra
Karacorlu, Murat
A case of morning glory syndrome associated with persistent hyperplastic primary vitreous and Peters’ anomaly
title A case of morning glory syndrome associated with persistent hyperplastic primary vitreous and Peters’ anomaly
title_full A case of morning glory syndrome associated with persistent hyperplastic primary vitreous and Peters’ anomaly
title_fullStr A case of morning glory syndrome associated with persistent hyperplastic primary vitreous and Peters’ anomaly
title_full_unstemmed A case of morning glory syndrome associated with persistent hyperplastic primary vitreous and Peters’ anomaly
title_short A case of morning glory syndrome associated with persistent hyperplastic primary vitreous and Peters’ anomaly
title_sort case of morning glory syndrome associated with persistent hyperplastic primary vitreous and peters’ anomaly
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244077/
https://www.ncbi.nlm.nih.gov/pubmed/28154792
http://dx.doi.org/10.3205/oc000053
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