Results 81 to 90 of about 14,669 (176)

[Morning glory syndrome].

Gaceta medica de Mexico, 2011
In 1970, Kindier described the morning glory syndrome. This syndrome is a congenital abnormality of the optic nerve with unilateral presence and very low incidence. It is characterized by an enlarged optical disc, deep excavation, presence of traces of radial glia, and arrangement of retinal vascularization.
Erika Paulina, López-Lizárraga, Rodrigo, Bolaños-Jiménez, M Guadalupe, Treviño-Alanís, Gerardo, Rivera-Silva   +3 more
openaire   +1 more source

Morning Glory Optic Syndrome

Medical Journal of Shree Birendra Hospital, 2006
Morning Glory Optic ...
openaire   +2 more sources

Refractory Central Serous Retinal Detachment in the Presence of Optic Disc Pit – Case Report

Okulistyka
Among congenital optic disc anomalies are megalopapilla, optic nerve aplasia and hypoplasia (de Morsier’s syndrome) and optic disc excavations. The latter are attributed to abnormal fetal fissure’s closure.
Radosław Kaczmarek, Dorota Kaczmarek
doaj   +1 more source

Bilateral morning glory disc anomaly with unilateral internal carotid artery agenesis

Indian Journal of Ophthalmology. Case Reports, 2022
Koyel Chakraborty, Sucheta Parija, Bhagabat Nayak, C. S Lalitha   +3 more
doaj   +1 more source

The Syndrome of Frontonasal Dysplasia, Callosal Agenesis, Basal Encephalocele, and Eye Anomalies – Phenotypic and Aetiological Considerations

International Journal of Medical Sciences, 2004
We report ten sporadic cases of Brazilian patients with facial midline defects, callosal agenesis, basal encephalocele, and ocular anomalies. This very rare cluster of anomalies has been well reported before. However, only until recently it is recognized
doaj  

Trades-offs between pollinator attraction and florivore defense maximize reproductive success in the self-incompatible Rivea ornata (Convolvulaceae)

BMC Ecology and Evolution
Background Rivea ornata, a rare species from the morning glory family, exhibits uncommon characteristics compared to other typical morning glories, including nocturnal flowers that fit the classic moth pollination syndrome.
Natthaphong Chitchak, Alyssa B. Stewart, Paweena Traiperm   +2 more
doaj   +1 more source

Case report: is there a link between morning glory syndrome and TANGO2 mutation disease, or is this an unusual association?

Neurología, 2022
J. Lobato Santos, F.J. Prieto López, M. R. Querol Pascual, B. Rebollo Lavado   +3 more
semanticscholar   +1 more source

Rare Triad of Midline Craniofacial Defects: A Case Report

Journal of Craniomaxillofacial Research
Midline craniofacial anomalies are rare malformations that may occur in isolation or as part of syndromic associations. Among them, the coexistence of basal encephalocele, agenesis of the corpus callosum, and Morning Glory Syndrome (MGS) is exceptionally
Praveen Thirumal, Ramakrishna N, Sai Praneetha Sagi   +2 more
doaj  

Bilateral morning glory syndrome associated with persistent fetal vasculature syndrome and corpus callosum agenesis: a case report

Oftalmologicheskii Zhurnal, 2021
N. Bobrova, T. Romanova, A. V. Shilik
semanticscholar   +1 more source

Intravitreal ranibizumab in the treatment of choroidal neovascularization secondary to morning glory syndrome in a child. [PDF]

Saudi J Ophthalmol, 2016
Özkaya A, Yilmaz I, Alkin Z, Karakucuk Y, Yazici AT.   +4 more
europepmc   +1 more source