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Miscellaneous (23)

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Abstract #69038 Published in IGR 18-1

Unilateral persistent fetal vasculature coexisting with anterior segment dysgenesia

Cañizares B; Yago I; Piñero Á; Ruiz M
Archivos de la Sociedad Española de Oftalmologia 2017; 92: 40-43

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CASE REPORT: A case is presented of a 4 week-old female neonate with Peters anomaly (PA) and unilateral persistent foetal vasculature (PFV) referred to our centre due to esotropia. At 12 weeks of age, a penetrating keratoplasty and vitrectomy were performed without major complications in the immediate post-operative period. The patient is currently under an intensive treatment for amblyopia and secondary glaucoma. DISCUSSION: Surgical treatment of PFV is controversial, with prevention of amblyopia, phthisis, and glaucoma being the main reasons for it. Patients with unilateral PFV and type II PA could be good candidates for this combined surgical procedure.

Unidad de Oftalmología Infantil, Servicio de Oftalmología, Hospital Virgen de la Arrixaca, Murcia, España. Electronic address: belen.nse@gmail.com.

Full article

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Classification:

9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (Part of: 9 Clinical forms of glaucomas > 9.1 Developmental glaucomas)
12.16 Vitrectomy (Part of: 12 Surgical treatment)
9.4.11.4 Glaucomas associated with corneal surgery (Part of: 9 Clinical forms of glaucomas > 9.4 Glaucomas associated with other ocular and systemic disorders > 9.4.11 Glaucomas following intraocular surgery)

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