Morning Glory Syndrome

Síndrome de Morning Glory

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Lizeth Pardo Hernández
Fabián Riaño Montañez

Abstract

Introduction: the congenital optic disc anomaly known as morning glory disc anomaly (MGDA) is an alteration of normal optic nerve development, characterized by an enlarged funnel-shaped cavity of the optic disc, the point in the eye where the optic nerve fibers leave the retina. The anomaly is typically unilateral. Most are isolated cases with no associated systemic anomalies. Objective: a case is presented in a one-year-old boy with MGDA and the corresponding imaging findings. Case reports: we present the case of a one-year-old male patient with suspected visual impairment. Cerebral magnetic resonance imaging (MRI) revealed a papillary funnel-shaped excavation in the left eye, alteration in the morphology and inferior asymmetric displacement of the optic chiasm and thickening of the pituitary infundibular stalk. Discussion: MGDA is diagnosed clinically, however, imaging provides additional information regarding the associated ocular, craniofacial and vascular abnormalities. In this case, in addition to the ocular lesion there were abnormalities of midline structures, such as, the pituitary infundibular stalk, as well as, optic chiasm thickening. Conclusion: imaging is fundamental, not only to describe the anatomic alteration of the optic nerve, but also to identify related abnormalities in order to provide patients a comprehensive management.

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Author Biographies

Lizeth Pardo Hernández, Fundación Universitaria de Ciencias de la Salud

Radiología e Imágenes Diagnósticas, Fundación Universitaria de Ciencias de la Salud, Bogotá DC, Colombia.

Fabián Riaño Montañez , Fundación Universitaria de Ciencias de la Salud

Neuroradiólogo, Hospital Infantil Universitario de San José, Fundación Universitaria de Ciencias de la Salud. Bogotá DC, Colombia.

References

Reis W. I. Eine wenig bekannte typische Missbildung am Sehnerveneintritt: Umschriebene Grubenbildung auf der Papilla n. optici. Eine wenig bekannte typische Missbildung am Sehnerveneintritt: Umschriebene Grubenbildung auf der Papillan. optici. Ophthalmologica. 1908;9:505–528. https://doi.org/10.1159/000291456 DOI: https://doi.org/10.1159/000291456

Kindler P. Morning glory syndrome: unusual congenital optic disk anomaly. Am J Ophthalmol. 1970;69(3):376-84. doi: 10.1016/00029394(70)92269-5 DOI: https://doi.org/10.1016/0002-9394(70)92269-5

Lee BJ, Traboulsi EI. Update on the morning glory disc anomaly. Ophthalmic Genet. 2008;29(2):47-52. doi:10.1080/13816810801901876 DOI: https://doi.org/10.1080/13816810801901876

Manschot WA. Morning glory syndrome: a histopathological study. Br J Ophthalmol. 1990;74(1):56-8. doi: 10.1136/bjo.74.1.56 DOI: https://doi.org/10.1136/bjo.74.1.56

Ellika S, Robson CD, Heidary G, Paldino MJ. Morning glory disc anomaly: characteristic MR imaging findings. AJNR Am J Neuroradiol. 2013;34(10):2010-4. doi: 10.3174/ajnr.A3542 DOI: https://doi.org/10.3174/ajnr.A3542

Ponnatapura J. Morning glory syndrome with Moyamoya disease: A rare association with role of imaging. Indian J Radiol Imaging. 2018;28(2):165-168. doi: 10.4103/ijri.IJRI_219_17 DOI: https://doi.org/10.4103/ijri.IJRI_219_17

Doneda C, Pinelli L, Scaramuzzi M, Galli J, Fazzi E, Parazzini C, et al. Morning Glory Disc Anomaly Associated with Ipsilateral Optic Nerve and Chiasm Thickening: Three Cases and Review of the Literature. Neuropediatrics. 2017;48(6):463-466. doi: 10.1055/s0037-1603642 DOI: https://doi.org/10.1055/s-0037-1603642

Ceynowa DJ, Wickström R, Olsson M, Ek U, Eriksson U, Wiberg MK, et al. Morning glory disc anomaly in childhood - a populationbased study. Acta Ophthalmol. 2015;93(7):626-634.doi: 10.1111/aos.12778 DOI: https://doi.org/10.1111/aos.12778

Thoma D, Nijs I, Demaerel P, Casteels I. Morning glory disc anomaly with an ipsilateral enlargement of the optic nerve pathway. Eur J Paediatr Neurol. 2017;21(5):787-91. doi: 10.1016/j.ejpn.2017.04.1334 DOI: https://doi.org/10.1016/j.ejpn.2017.04.1334

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