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Welcome to the new AJNR, Updated Hall of Fame, and more. Read the full announcements.


AJNR is seeking candidates for the position of Associate Section Editor, AJNR Case Collection. Read the full announcement.

 

Case of the Week

Section Editors: Matylda Machnowska1 and Anvita Pauranik2
1University of Toronto, Toronto, Ontario, Canada
2BC Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada

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Submit a Case Previous Cases ASPNR Pediatric Cases

March 26, 2015
  • Description
  • Legends
  • Diagnosis
  • Brain Teaser
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Basal Encephalocele and Morning Glory Syndrome

  • Morning glory syndrome (MGS) is a congenital malformation of the optic disc.
  • Basal (meningo) encephalocele is a sporadic and occult malformation, described in 67.7% of MGS patients, usually associated with midline defects such as cleft palate and corpus callosum agenesis, optic disc, and other brain anomalies. Sella abnormalities are often seen.
  • MGS manifests with a broad spectrum of characteristics. It is usually a nonprogressive, untreatable disease. Accurate diagnosis is important due to its association with systemic anomalies and increased incidence of retinal detachment. Dysplasic optic disc should always alert physicians to evaluate for an encephalocele and sella abnormalities.

Suggested Reading

Naidich TP, Altman NR, Braffman BH, et al. Cephaloceles and related malformations. AJNR Am J Neuroradiol 1992;13:655–90

Morioka M, Murabayashi T, Masumitsu T, et al. Basal encephaloceles with morning glory syndrome, and progressive hormonal and visual disturbances: case report and review of the literature. Brain Dev 1995;17:196–201

Current Issue

American Journal of Neuroradiology: 45 (12)
American Journal of Neuroradiology
Vol. 45, Issue 12
1 Dec 2024
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Print ISSN: 0195-6108 Online ISSN: 1936-959X

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