Abstract

PurposeTo report the clinical and echographic features, the prevalence of retinal detachment (RD), and associated visual acuity in a cohort of pediatric patients with morning glory disc anomaly (MGDA).MethodsThis was a retrospective review of 249 pediatric patients with MGDA (271 eyes) seen at the Dept. of Ophthalmology, Xinhua Hospital. Their medical records were reviewed for demographic data and ocular and systemic findings. The maximal depth and width of the cavity were measured using standardized echographic images. The ratios of cavitary depth to axial length, cavitary depth to maximal cavitary width, and the product of cavitary depth and width were calculated and used to indicate the relative size of the excavation. The clinical and echographic findings were correlated with visual acuity and the occurrence of RD of the patient.ResultsThe relative size of the excavation and the presence of RD were positively associated with increased risk of poor vision (p < 0.05). The presence of persistent fetal vasculature was not associated with the risk of RD and poor vision. The ratio of cavitary depth to axial length more than or equal to 0.25 conferred an increased risk of RD (OR, 2.101; 95% CI, 1.469–3.003).ConclusionsClinical and echographic features of MGDA may be used in predicting the risk of RD. Measuring the relative size of excavation via echography may guide the follow-ups and assist in the early diagnosis of RD.

Highlights

  • Morning glory disc anomaly is a rare congenital cavitary anomaly of the optic disc, characterized by an enlarged and excavated optic disc with juxtapapillary chorioretinal pigment disturbance, radial retinal blood vessels, and a central white glial tuft

  • Eyes with MGDA and persistent fetal vasculature (PFV) have been well-described by Fei et al [8], which showed a high occurrence of ocular complications

  • We evaluated the excavation in a cohort of 271 MGDA eyes based on ocular echography using a method proposed by Venincasa et al for ocular coloboma [12]

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Summary

Introduction

Morning glory disc anomaly is a rare congenital cavitary anomaly of the optic disc, characterized by an enlarged and excavated optic disc with juxtapapillary chorioretinal pigment disturbance, radial retinal blood vessels, and a central white glial tuft. Patients with MGDA often have other abnormalities Ocular complications, such as persistent fetal vasculature (PFV), cataracts, microphthalmia, and retinal detachment (RD), are frequently found in MGDA eyes. Systemic disorders, such as Aicardi syndrome, basal encephalocele, persisting embryonal infundibular recess, and other cerebrovascular anomalies, have been reported together with MGDA [2, 4–7]. Studies on visual prognosis of MGDA eyes with variable clinical features are rare

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