Results 91 to 100 of about 835,973 (179)
"Morning Glory" disc. Note tapering edge pointing to basal encephalocele. Boy.
William F. Hoyt, MD
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Morning Glory Disc Anomaly in a Child with Esotropia [PDF]
Ilias Georgalas +3 more
openaire +3 more sources
Cavitary anomalies of the optic disc: neurologic significance
Cavitary congenital optic disc anomalies include optic disc coloboma, morning glory disc anomaly, optic pit, and the papillorenal syndrome. Peripapillary staphyloma is occasionally included in this group but it does not represent an anomaly of the optic ...
Golnik, Karl C
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Salt-and-pepper-like retinopathy in a case of morning glory disc anomaly. [PDF]
Kumawat D, Patel S, Sachan A, Sahay P.
europepmc +1 more source
Morning glory optic disc anomaly associated with retinal detachment in a 9-year-old northern Nigerian male child: a case report [PDF]
Morning glory syndrome (MGS) is uncommon in Nigeria as is less commonly seen in Africans. It is one of the congenital excavated optic disc dysplasia apart from optic disc coloboma and peripapillary staphyloma.
Sani, Rabi Y. +6 more
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Optic Nerve Abnormalities in Morning Glory Disc Anomaly: An MRI Study
Background: The morning glory disc anomaly (MGDA) is a rare congenital malformation of the optic disc. The association with a significant enlargement of the optic nerve has been recently reported in a few cases, raising the question of potentially ...
Diem-Trang Nguyen; Nathalie Boddaert; Dominique Bremond-Gignac; Matthieu P. Robert
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We present a 51-year-old female with a unilateral congenital excavated optic discanomaly. After clinical examination and appropriate diagnostic procedures wewere unable to determine with certainty whether it is a morning glory anomaly or aperipapillary ...
Mavija, Milka +2 more
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Computerized Tomography of Two Patients with Morning Glory Syndrome [PDF]
Morning glory syndrome (MGS), an uncommon optic disc anomaly, is characterized by a funnel-shaped, excavated optic disc surrounded by chorioretinal pigmentary disturbance. Generally, it is an isolated ocular abnormality. The authors describe two patients
Sakata, Hiroshi +4 more
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