scholarly journals Hypothalamic Hypopituitarism Presenting with Pituitary Malformation and Morning Glory Syndrome: A Case Report

2005 ◽  
Vol 14 (Supplement24) ◽  
pp. S24_97-S24_100
Author(s):  
Kaori Kinoshita ◽  
Itsuro Kazukawa ◽  
Yuji Hashimoto ◽  
Hideki Uchikawa ◽  
Yoshinori Morita ◽  
...  
Keyword(s):  
Case Report ◽  
Morning Glory ◽  
Morning Glory Syndrome

Choroidal Neovascularization Associated with Morning Glory Syndrome: A Case Report

2020 ◽  
Vol 04 (06) ◽  
Author(s):  
Shigeru Sato ◽  
Takeshi Morimoto ◽  
Sayaka Tanaka ◽  
Motokazu Tsujikawa ◽  
Kohji Nishida
Keyword(s):  
Case Report ◽  
Choroidal Neovascularization ◽  
Morning Glory ◽  
Morning Glory Syndrome

Case report: The morning glory syndrome

1990 ◽  
Vol 73 (1) ◽  
pp. 31-35 ◽  
Author(s):  
Shane Debney ◽  
Algis J. Vingrys
Keyword(s):  
Case Report ◽  
Morning Glory ◽  
Morning Glory Syndrome

scholarly journals Morning Glory Syndrome: a Case Report

2018 ◽  
Author(s):  
Rodrigo Martins ◽  
Stephanie de Farias ◽  
Henrique Martins ◽  
Ingrid do Couto ◽  
Marcos da Silva Souza ◽  
...  
Keyword(s):  
Case Report ◽  
Morning Glory ◽  
Morning Glory Syndrome

scholarly journals Bilateral Morning Glory Syndrome with Bilateral Persistent Fetal Vasculature in a Patient with Joubert’s Syndrome

2020 ◽  
Vol 2020 ◽  
pp. 1-5
Author(s):  
Ahmad Bilal Araissi ◽  
Alaa Fayed ◽  
Youssef Helmy
Keyword(s):  
Case Report ◽  
Optic Disc ◽  
Fibrous Tissue ◽  
Morning Glory ◽  
Persistent Fetal Vasculature ◽  
Morning Glory Syndrome ◽  
First Case ◽  
Ophthalmologic Examination ◽  
The Brain ◽  
Delayed Growth

Purpose. We report a case of a 1-year-old girl who was referred to us with a cerebellar anomaly and delayed growth and development for bilateral ptosis and poor fixation. Based on our ophthalmologic examination, we concluded that she has bilateral persistent fetal vasculature (PFV) with morning glory syndrome (MGS). A closer look into her neurologic condition revealed that she has Joubert’s syndrome. Observations. External examination revealed bilateral symmetrical ptosis with syndromic facies and her fundus examination revealed a large dysplastic optic disc with anomalous radiating vessels and a fibrous tissue tuft originating from the disc. The left eye showed similar findings in addition to a central excavation and a fibrovascular stalk extending from the optic disc. These findings were consistent with bilateral MGS and bilateral PFV. The brain imaging included a computed tomography scan and magnetic resonance imaging, both of which revealed a “molar tooth appearance” of the midbrain and an anomalous cerebellum suggestive of Joubert’s syndrome. Conclusions and Importance. This is the first case report of a case of bilateral MGS and bilateral PFV associated with Joubert’s syndrome. This case report documents the associated optic nerve disease in these patients, not previously described, which are additive causes of visual compromise in addition to the brain insult.

scholarly journals Morning Glory Syndrome in Two (02) Malians: Case Report from IOTA-University Hospital

2020 ◽  
Vol 10 (03) ◽  
pp. 255-259
Author(s):  
Seydou Bakayoko ◽  
Brainima Coulibaly ◽  
Mohamed Kolé Sidibe ◽  
Elien Gyrr ◽  
Modibo Sissoko ◽  
...  
Keyword(s):  
Case Report ◽  
Morning Glory ◽  
University Hospital ◽  
Morning Glory Syndrome

scholarly journals Basal encephalocele associated with morning glory syndrome: case report

2007 ◽  
Vol 65 (4a) ◽  
pp. 988-991 ◽  
Author(s):  
Ivanete Minotto ◽  
Nitamar Abdala ◽  
Adriana Aparecida Siviero Miachon ◽  
Angela Maria Spinola e Castro ◽  
Paulo Imamura ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Computed Tomography ◽  
Case Report ◽  
Magnetic Resonance ◽  
Brain Tissue ◽  
Morning Glory ◽  
Resonance Imaging ◽  
Pituitary Dwarfism ◽  
Morning Glory Syndrome ◽  
Basal Encephalocele

The basal encephaloceles refer to rare entities and they correspond to herniation of brain tissue through defects of skull along the cribiform plate or the sphenoid bone. A rare morning glory syndrome, with characteristic retinal defect has been reported in association with basal encephaloceles. Hypophysis hormonal deficiencies may occur. We accounted for a pituitary dwarfism with delayed diagnosed transsphenoidal encephalocele associated with morning glory syndrome, showing the alterations found in retinography, computed tomography and magnetic resonance imaging.

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