A rare association of blepharophimosis–ptosis–epicanthus inversus syndrome with unilateral posterior persistent fetal vasculature

Blepharophimosis–ptosis–epicanthus inversus syndrome (BPES) is a rare genetic syndrome characterized by dysmorphism of ocular adnexa. We report a rare presentation of BPES and posterior persistent fetal vasculature (PFV) in a 10-year-old male child. A thorough evaluation showed all the classical fea...

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Auteurs principaux:	Syed W A Rizvi, Iraj A Khan, Syed M D Qaseem, Syed A R Rizvi, Mohammed A Siddiqui, Pragya Ahuja
Format:	Artigo
Langue:	Inglês
Publié:	Wolters Kluwer Medknow Publications 2023-07-01
Collection:	Indian Journal of Ophthalmology. Case Reports
Sujets:	bpes congenital malformations pfv surgical challenge
Accès en ligne:	https://journals.lww.com/10.4103/IJO.IJO_81_23
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