Relevant bibliographies by topics / Ocular malformations

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters

Academic literature on the topic 'Ocular malformations'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Ocular malformations"

1

Daglio, Daniel Eduardo, Micaela De Lucía, David Gwyn Robinson, and Diego Eduardo Gutiérrez Gregoric. "Ocular tentacle malformation in Deroceras reticulatum (Mollusca: Gastropoda: Agriolimacidae)." Papéis Avulsos de Zoologia 59 (August 15, 2019): e20195932. http://dx.doi.org/10.11606/1807-0205/2019.59.32.

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Malformations in animals have long been known. In gastropod, natural and induced malformations are mentioned in different systems and in ocular tentacles, mainly linked to cases of parasitism and exposure to pollutants (molluscicides and chemicals). In this study we present a new malformation not documented in the ocular tentacles of slug Deroceras reticulatum that could be due to the action of pesticides. This malformation in D. reticulatum is the first malformation to be mentioned for South America in nursery gardens.
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Guarnera, Alessia, Paola Valente, Luca Pasquini, et al. "Congenital Malformations of the Eye: A Pictorial Review and Clinico-Radiological Correlations." Journal of Ophthalmology 2024 (January 30, 2024): 1–17. http://dx.doi.org/10.1155/2024/5993083.

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Congenital malformations of the eye represent a wide and heterogeneous spectrum of abnormalities that may be part of a complex syndrome or be isolated. Ocular malformation severity depends on the timing of the causative event during eye formation, ranging from the complete absence of the eye if injury occurs during the first weeks of gestation, to subtle abnormalities if the cause occurs later on. Knowledge of ocular malformations is crucial to performing a tailored imaging protocol and correctly reporting imaging findings. Together with the ophthalmologic evaluation, imaging may help frame oc
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3

Buyse, Gunnar, Lieven Lagae, Philippe Demaerel, Frank Kesteloot, Ingele Casteels, and Louise Knoors. "A Conjunctival Vascular Malformation as a Rare Presenting Sign of Wyburn–Mason Syndrome." Journal of Pediatric Neurology 16, no. 04 (2017): 239–42. http://dx.doi.org/10.1055/s-0037-1607996.

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AbstractWyburn–Mason syndrome is a rare condition that is characterized by ipsilateral arteriovenous malformations affecting the eye, brain, and facial skin. A conjunctival vascular dilation can be a rare ocular presenting sign. We report a 6-year-old boy who attended the hospital because of the sudden appearance of a conjunctival vascular lesion in his right eye. Inspection of his facial skin showed a subtle discoloration along the right trigeminal nerve and a vascular structure of the conjunctiva. Fundoscopy showed dilated and tortuous retinal vessels. Brain magnetic resonance imaging (MRI)
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Warburg, M. "Ocular malformations and lissencephaly." European Journal of Pediatrics 146, no. 5 (1987): 450–52. http://dx.doi.org/10.1007/bf00441592.

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Strömland, Kerstin. "Ocular malformations with embryonic implications." Acta Ophthalmologica Scandinavica 73, S214 (2009): 9–11. http://dx.doi.org/10.1111/j.1600-0420.1995.tb00580.x.

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Radić Nišević, Jelena, Igor Prpić, Ronald Antulov, Antun Sasso, and Izidora Holjar Erlić. "Encephalocraniocutaneous Lipomatosis Without Ocular Malformations." Pediatric Neurology 60 (July 2016): 71–74. http://dx.doi.org/10.1016/j.pediatrneurol.2016.03.005.

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Traboulsi, Elias I. "Ocular malformations and developmental genes." Journal of American Association for Pediatric Ophthalmology and Strabismus 2, no. 6 (1998): 317–23. http://dx.doi.org/10.1016/s1091-8531(98)90024-6.

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Zetterström, Birgitta. "OCULAR MALFORMATIONS CAUSED BY THALIDOMIDE." Acta Ophthalmologica 44, no. 3 (2009): 391–95. http://dx.doi.org/10.1111/j.1755-3768.1966.tb08048.x.

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İlker, S. Sami, Abdullah Ceylan, Kazım Aral, and Necdet Bekir. "Ocular Traumas and Conjunctival Flora in Newborns, Comparing with the Maternal Vaginal Flora." European Journal of Therapeutics 2, no. 2 (1991): 150–57. http://dx.doi.org/10.58600/eurjther.19910202-527.

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The purpose of this study is to analyze the data concerning ocular injuries, congenital abnormalities, and the conjunctival flora of newborns. For this reason, randomised 224 newborns at Ankara Central Maternity Hospital were examined. We found 2,2 percent ocular congenital malformations and abnormalities 2,6 percent extraocular congenital malformation and abnormalities among these babies. The fewest lesions have been met in those delivered by the Cesarian section, and all delivered that were made by forceps and other equipment have had some lesions depending on the birth trauma. We also found
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Mohamed, Abdallahi Ould Hamed. "Bilateral iris, lens and Chorioretinal Coloboma: A Case Report." Journal of Clinical Research and Ophthalmology 5, no. 1 (2018): 012. https://doi.org/10.17352/2455-1414.000047.

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Colobomas are genetic malformations due to lack of closure of the embryonic fissure. These are rare malformations that can sit at any level of the eye. Colobomas can be uni or bilateral, sporadic or hereditary. It may be associated with other ocular manifestations and extra-ocular malformations involving a general, clinical and radiological examination. We report the case of a 28 year old young man with no significant pathological history whose ophthalmological examination revealed a coloboma affecting the iris, lens and choroid.
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Dissertations / Theses on the topic "Ocular malformations"

1

Teär, Fahnehjelm Kristina. "Posterior ocular malformations in children : teratological aspects /." Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-470-4.

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Saraiva, Inês Quintão. "Malformações oculares congénitas em cães e gatos : estudo de 123 casos." Master's thesis, Universidade de Lisboa, Faculdade de Medicina Veterinária, 2019. http://hdl.handle.net/10400.5/18034.

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Dissertação de Mestrado Integrado em Medicina Veterinária<br>As malformações oculares congénitas são alterações raras que ocorrem por defeitos no desenvolvimento ocular embrionário, que podem surgir espontaneamente ou ser induzidas por fatores teratogénicos durante a gestação, incluindo fatores genéticos e não genéticos. Podem afetar um ou ambos os olhos e surgir isoladamente ou de forma combinada. O presente estudo teve como principais objetivos determinar qual a prevalência das malformações oculares congénitas em cães e gatos e quais as mais frequentemente diagnosticadas em cada espécie. A
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3

Chassaing, Nicolas. "Génétique des micro-anophtalmies : revue des phénotypes et des génotypes : stratégies d'identification de nouveaux gènes impliqués dans le développement oculaire." Toulouse 3, 2013. http://thesesups.ups-tlse.fr/2551/.

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Les anophtalmies et microphtalmies (AM) sont les plus sévères des malformations de l'œil. Les causes d'origine génétique sont prépondérantes, mais une cause moléculaire ne peut être identifiée que chez environ 25 % des patients. Nous avons étudié la fréquence des mutations des principaux gènes d'AM dans une large cohorte de 150 patients et défini la variabilité phénotypique associée à ces mutations. Pour découvrir de nouveaux gènes d'AM, différentes approches ont été utilisées: gènes candidats, CGH-array, et approche fondamentale (transcriptomique, ChIP, séquençage haut débit). Nous avons ains
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Rooryck, Thambo Caroline. "Analyse de réarrangements génomiques chez des patients atteints d'anomalies du développement embryonnaire : retard mental et malformations multiples congénitales; spectre oculo-auriculo-vertébral." Thesis, Bordeaux 2, 2009. http://www.theses.fr/2009BOR21675/document.

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Notre travail s’est intéressé aux anomalies du développement embryonnaire d’origine génétique en étudiant : -d’une part des patients associant des malformations congénitales multiples plus ou moins associées à un retard mental et à un syndrome dysmorphique, -et d’autre part des patients présentant un phénotype particulier : le spectre oculo-auriculo-vertébral (OAVS) incluant le syndrome de Goldenhar. L’analyse a consisté en l’étude pangénomique de ces patients au moyen de puces à ADN (CGH-array), dans le but d’identifier de nouveaux remaniements chromosomiques avec anomalie du nombre de copies
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Trimouille, Aurélien. "Décryptage des mécanismes moléculaires menant au Spectre Oculo-Auriculo-Vertébral : de la recherche de gène aux modèles animaux." Thesis, Bordeaux, 2020. http://www.theses.fr/2020BORD0336.

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Le syndrome de Goldenhar, ou spectre Oculo-Auriculo-Vertébral (OAVS [MIM: 164210]), est une anomalie du développement embryonnaire associant des malformations des structures dérivées des premier et second arcs branchiaux, notamment l'oreille, l'œil, la mandibule et les vertèbres. Il s’agit du deuxième spectre malformatif embryonnaire le plus fréquent de la tête et du cou. Le phénotype clinique esthétérogène et caractérisé par une microsomie hémifaciale, des anomalies auriculaires asymétriques, des dermoïdes épibulbaires, et des malformations vertébrales.Différentes causes non génétiques ont ét
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Books on the topic "Ocular malformations"

1

De Laey, J. J., and M. Hanssens. Vascular Tumors and Malformations of the Ocular Fundus. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0589-4.

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2

M, Hanssens, and Belgian Ophthalmological Society, eds. Vascular tumours and malformations of the ocular fundus. Kluwer Academic Publishers, 1990.

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3

Laey, J. J. De. Vascular tumors and malformations of the ocular fundus. Kluwer Academic Publishers, 1990.

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4

Martyn, Lois J. Optic fundus signs of developmental and neurological disorders in children: A manual for clinicians. Spastics International Medical Publications ; Philadelphia : Lippincott, 1985.

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Martyn, Lois J. Optic fundus signs of developmental and neurological disorders in children: A manual for clinicians. Spastics International Medical Publications, 1985.

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6

Laey, J. J. de. Vascular Tumors and Malformations of the Ocular Fundus. Springer, 2011.

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7

Hanssens, M., and J. J. de Laey. Vascular Tumors and Malformations of the Ocular Fundus. Springer, 2012.

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Vascular Tumors and Malformations of the Ocular Fundus. Springer, 2011.

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9

Soleta, Amy, and Joelle Karlik. Goldenhar Syndrome. Edited by Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi, and Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0058.

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Goldenhar syndrome (also known as oculo-auriculo-vertebral spectrum, facio-auriculo-vertebral syndrome, and Goldenhar-Gorlin syndrome) is caused by fetal growth disturbances of the first two brachial clefts. Diagnostic criteria include eye, ear, mandibular, and/or vertebral anomalies. These patients may also have cardiac and renal malformations with varying degrees of severity. Airway management for Goldenhar patients may include difficult ventilation and intubation, which may become increasingly difficult with age. Vertebral anomalies including fused cervical vertebrae and/or cervical instabi
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Martyn, Lois J., Anthony J. Pileggi, and Henry W. Baird. Optic Fundus Signs of Developmental and Neurological Disorders in Children: A Manual for Clinicians (Clinics in Developmental Medicine (Mac Keith Press)). Cambridge University Press, 1991.

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Book chapters on the topic "Ocular malformations"

1

Piozzi, Elena, and Alessandra Del Longo. "Ocular Malformations." In Neonatology. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-29489-6_282.

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Piozzi, Elena, and Alessandra Del Longo. "Ocular Malformations." In Neonatology. Springer Milan, 2012. http://dx.doi.org/10.1007/978-88-470-1405-3_145.

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Piozzi, Elena, and Alessandra Del Longo. "Ocular Malformations." In Neonatology. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-18159-2_282-1.

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Wall, Palak B., and Elias I. Traboulsi. "Optic Nerve Malformations." In Practical Management of Pediatric Ocular Disorders and Strabismus. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-2745-6_38.

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De Laey, J. J., and M. Hanssens. "Choroidal hemangioma." In Vascular Tumors and Malformations of the Ocular Fundus. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0589-4_1.

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De Laey, J. J., and M. Hanssens. "Coats’ syndrome and retinitis pigmentosa." In Vascular Tumors and Malformations of the Ocular Fundus. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0589-4_10.

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De Laey, J. J., and M. Hanssens. "Presumed acquired retinal angiomatosis (Adult Coats’ disease)." In Vascular Tumors and Malformations of the Ocular Fundus. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0589-4_11.

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De Laey, J. J., and M. Hanssens. "Acquired retinal macroaneurysms." In Vascular Tumors and Malformations of the Ocular Fundus. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0589-4_12.

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De Laey, J. J., and M. Hanssens. "Retinal angiomatosis — von Hippel-Lindau’s Disease." In Vascular Tumors and Malformations of the Ocular Fundus. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0589-4_2.

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De Laey, J. J., and M. Hanssens. "Capillary Hemangioma of the optic disc." In Vascular Tumors and Malformations of the Ocular Fundus. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0589-4_3.

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