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Morning glory syndrome retinal detachment

Vitrectomy of rhegmatogenous retinal detachment in morning

  1. Morning glory syndrome is a rare congenital anomaly with the optic nerve. Many ocular abnormalities have been reported. These include strabismus, cataract, nystagmus, lens coloboma, eye lid hemangioma, aniridia, microph-thalmos, Duane's retraction syndrome and retinal detachment-
  2. We report a case of morning glory disc anomaly in a young patient with tractional retinal detachment successfully repaired with complex pars plana vitrectomy, membrane peel, laser, and oil tamponade. A 19-year-old female with a history of right morning glory disc anomaly associated with PAX6 gene mu
  3. Morning glory syndrome is typically unilateral with equal involvement of the right and left eyes. Bilaterality of this condition can occur. 4 The visual prognosis is usually poor, in the 20/100 to 20/200 range. Serous retinal detachments can occur in 30% of individuals
  4. iscent of the morning glory flower. 1 Up to 38% of cases exhibit retinal detachment, the origin of which is controversial. It is believed that the.
  5. A 2-year-old-girl had a MGS with a large hole in the excavated disc and retinal detachment. The visual acuity was 4/200 in the affected eye. The excavated disc and retinal detachment were con-firmed by echogram. Optical coherence tomography demonstrated that the large hole was connected to the subretinal space
  6. DISCUSSION Retinal detachment is an intriguing finding in association with the morning glory optic disk anomaly. 9,10 Of 32 patients described by Haik and associates, 11 had retinal detachments. Ten of these detachments were nonrhegmatogenous; Fig. 3 (Chang and associates)

Morning glory syndrome (MGS) is a birth (congenital) defect of the nerve of the eye (optic nerve) that resembles a flower known as morning glory. It is characterized by an enlarged, funnel-shaped cavity of the optic disc, the point in the eye where the optic nerve fibers leave the retina Rhegmatogenous retinal detachment in morning glory syndrome pathogenesis and treatment. Int Ophthalmol . 2001; 24(1): 21-4. 15 Chang S, Gregory-Roberts E, Chen R. Retinal detachment associated. Morning glory syndrome (MGS) is a congenital optic disc anomaly. It was named by Peter Kindler who observed that the fundus resembled a blossoming morning glory [ 1 ]. The prevalence of MGS has been reported to be 2.6/100,000 [ 2 ]. The pathogenesis of this congenital defect is not fully understood [ 3 ] Retinal Detachment Surgery in Morning Glory Syndrome. Atul Dhawan, MD. Dr. Dhawan performs surgery on an 8-year-old girl presenting with Morning Glory Syndrome and retinal detachment in her left eye. Posted: 10/28/201

RETINAL DETACHMENT IN MORNING GLORY SYNDROME TREATED BY TRIAMCINOLONE ACETONIDE-ASSISTED PARS PLANA VITRECTOMY. From the Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan. RETINA,™ The Journal of Retinal and Vitreous Diseases, encourages authors to submit Brief Reports describing unusual. A case of bilateral Morning Glory syndrome is presented, unusual because of a rhegmatogenous posterior pole retinal detachment in the left eye. Posterior pole retinal detachments have been described in association with this syndrome. This case report is the first presentation of a retinal tear located within the excavation surrounding the. An increased risk of retinal detachment has been seen in individuals with Morning Glory Syndrome. Retinal detachment causes the separation of the photosensitive layer of the eye, called retina, from the back layers of the eyeball. Retinal detachment is a surgical emergency, which can cause blindness, if it is not treated immediatel Colobomatous optic disc anomalies, including optic disc colobomas and morning glory syndrome, are uncommon, and sometimes associated with retinal detachment and/or retinoschisis. In optic disc..

A series of optic disc coloboma and morning glory syndrome cases demonstrated a retinal break within a peripapillary defect in 5 of 6 cases. Retinal detachment was less likely to occur, remained subclinical, or spontaneously resolved in the absence of vitreous or glial tissue causing retinal traction within the anomaly (1984): Retinal detachment in morning glory syndrome. Ophthalmic Surg 15: 841-843. Bartz-Schmidt KU & Heimann K (1995): Pathogenesis of retinal detachment asso-ciated with morning glory disc. Int Ophthalmol 19: 35-38. Chang S, Haik BG, Ellsworth RM, Louis LS & Berrocal JA (1984): Treatment of total retinal detachment in morning glory syn-drome Purpose: Morning glory disc anomaly (MGDA) is associated with a high prevalence of retinal detachment (RD), sometimes requiring multiple surgeries. The study aimed to establish the outcomes of RD..

Fundus image of a 7-year-old patient status post Vitrectomy and Silicone oil insertion in a case of Retinal detachment with Morning glory Syndrome. Photographer: Dr Shobhit Chawla, Prakash Netra Kendr, Lucknow, UP, INDIA. Imaging device: Zeiss Clarus. Condition/keywords: Morning Glory Syndrome, retinal detachment, silicone oi Background: The pathogenesis of non-rhegmatogenous retinal detachment (non-RRD) associated with morning glory syndrome (MGS) is not established, as well as best surgical approach to treat RD Retinal detachment (RD) is the most serious retinal complication of morning glory disc anomaly, with an incidence of 14% to 37%. 1-4 The pathogenesis is speculated to involve a juxtapapillary retinal break or abnormal communication between the subarachnoid space and subretinal space. 2 Spontaneous retinal reattachment can occur in up to 36% of.

Management of Retinal Detachment Associated with Morning

  1. We report a case of morning glory syndrome with retinal detachment. A slit-like retinal break at the edge of the excavated disc anomaly provided a direct communication between the subretinal space and the vitreous cavity. Retinal reattachment and useful vision was achieved after a single procedure of vitrectomy and gas tamponade. We believe that identification of the retinal break, removal of.
  2. The morning glory optic disc abnormality or morning glory syndrome (MGS), that is also known as Handmann'sches Anomaly, is a congenital malformation of the intraocular and intrascleral parts of the optic nerve associated with a colobomatous defect of the optic nerve head [1-5]
  3. Cases and Findings : Morning glory syndrome with retinal detachment was present in a 8-year-old girl, 16-year-old female and 23-year-old male. All were unilaterally affected and showed extensive retinal detachment involving the macula. All the 3 eyes received vitreous surgery
  4. Morning glory syndrome is a congenital optic disc anomaly in which much of the excavated colobomatous optic disc is filled with glial tissue. Ocular complications may include strabismus, reduced visual acuity and retinal detachment it may have systemic associations as in Aicardi's syndrome. A patient with monocular morning glory syndrome

Morning Glory Syndrome, retinal detachment, silicone oil Photographer Dr Shobhit Chawla, Prakash Netra Kendr, Lucknow, UP, INDIA Imaging device Fundus camera Zeiss Clarus Description Fundus image of a 7-year-old patient status post Vitrectomy and Silicone oil insertion in a case of Retinal detachment with Morning glory Syndrome.. Rhegmatogenous retinal detachment in Morning Glory Syndrome - pathogenesis and treatment Rhegmatogenous retinal detachment in Morning Glory Syndrome - pathogenesis and treatment Ho, Cheng-Lien; Wei, Li-Chen 2004-10-17 00:00:00 We report a case of morning glory syndrome with retinal detachment. A slit-like retinal break at the edge of the excavated disc anomaly provided a direct. Introduction. The morning glory syndrome (MGS) or morning glory disc anomaly was named by Kindler in 1970 because of its resemblance to the morning glory flower.1 It is a congenital, funnel-shaped excavation of the posterior fundus that incorporates the optic disc, with a white tuft of glial tissue overlying the central portion of the disc and the increased number of blood vessels arising from.

Morning glory syndrome is a relatively rare congenital optic disc anomaly that is often difficult to identify when associated with additional congenital ocular anomalies. This case report describes the diagnosis, treatment, and postoperative follow-up care of a young girl with morning glory syndrome accompanied by persistent fetal vasculature, retinal fold, and retinal detachment Morning glory syndrome (MGS) is a congenital optic disc anomaly that can be discovered at any age, though most patients are usually made aware of the condition at their first eye examination. Retinal detachment may develop during the clinical course. 15-21 Strabismus is frequently encountered in patients with MGS as well. 22. Many ocular.

Pars plana vitrectomy was performed on a six-year-old boy with complete retinal detachment associated with a morning glory disc of his left eye. Perfluorodecalin was injected to unfold the retina. During surgery, perfluorodecalin leaked repeatedly under the retina. This case demonstrates that a retinal hole in tissues lying within the optic disc anomaly provides a communication for fluid and. 9. Jo YJ, Iwase T, Oveson BC, et al. Retinal detachment in morning glory syndrome with large hole in the excavated disc. Eur J Ophthalmol. 2011;21(6):841−844. 10. Ho TC, Tsai PC, Chen MS, et al. Optical coherence tomography in the detection of retinal break and management of retinal detachment in morning glory syndrome To the best of our knowledge, treatment of serous retinal detachment in morning glory syndrome 2 with acetazolamide has not been previously reported. Improvement in visual acuity and significant.

There is a pretty significant increase to the risk of retinal detachment, but there isn't anything you can do about that other than monitor your eye health regularly and treat it if it happens. 1. Reply. Share. Report Save. level 1 · 3m. Hey, i'm 21 and i was diagnosed with unilateral Morning glory syndrome in my left eye when i was 6 years. Morning Glory Syndrome Definition. Morning glory syndrome (MGS) is an optic neuropathy characterized by a congenital funnel shaped excavation of the posterior fundus that incorporates the optic disc malformation (resembling the morning glory flower) MGS is usually unilateral and may result in a decrease in best-corrected visual acuity (BCVA) Sakamoto M, Kuniyoshi K, Hayashi S, Yamashita H and Kusaka S (2020) Total retinal detachment and contractile movement of the disc in eyes with morning glory syndrome, American Journal of Ophthalmology Case Reports, 10.1016/j.ajoc.2020.100964, 20, (100964), Online publication date: 1-Dec-2020 The chorioretinal changes may include optic disc coloboma (50 per cent of cases), morning glory syndrome, optic nerve hypoplasia, iris and choroidal colobomata and retinal detachment. Second example is Moyamoya disease, an association between morning glory disk anomaly (MGDA) and intracranial vascular anomalies[ 7 ]

Morning glory syndrome (MGS) is a congenital optic disc anomaly caused by abnormal closure of the embryonic fissure. Retinal detachment is commonly associated with MGS, though the association of choroidal neovascularization (CNV) with MGS is rare. Herein, we report a case of CNV associated with MGS, which wa Communication between the subretinal space and the vitreous cavity in the morning glory syndrome. Graefe's Archive for Clinical and Experimental Ophthalmology, 1996. Gary Brown. K. Bartz-schmidt. G. Coll. S. Chang. Tom Flynn. Gary Brown. K. Bartz-schmidt. G. Coll Morning glory disk anomaly is generally a unilateral, sporadic congenital abnormality of the optic disk. These eyes are at risk of developing retinal detachment requiring surgical repair. The etiology of retinal detachment is incompletely understood in this condition and some reports have attributed it to a retinal break. We report an unusual case of morning glory disk anomaly with total. Examination was remarkable for a cataract and complete retinal detachment in the left eye, with a markedly escavated, pale, funnel-shaped optic disc in the contralateral eye, with the depression extending to the macular area. The findings were compatible with morning-glory syndrome, with macular involvement Morning glory syndrome (MGS) is a congenital optic disc anomaly caused by abnormal closure of the embryonic fissure. Retinal detachment is commonly associated with MGS, though the association of choroidal neovascularization (CNV) with MGS is rare. Herein, we report a case of CNV associated with MGS, which was successfully treated with a single.

Morning Glory Syndrome - American Academy of Ophthalmolog

Retinal detachment associated with Morning Glory syndrome

Retinal detachment involved the temporal fundus and the macula in the right eye. A tear was present in the temporal periphery. The retina became reattached after buckling with final visual acuity of 0.03. Conclusion: The present cases show that retinal detachment in morning glory syndrome may show retinal breaks and is to be surgically treated Combined Optical Coherence Tomography and Ultrasound assisted analysis for retinal detachment in morning glory syndrome Abstract: Optical imaging for biological tissue is of great interest in the biomedical field because of its many qualities. the use of the waves between the visible and the infrared makes the optical imaging noninvasive and.

Retinal Detachment in Morning Glory Syndrome with Large

Signs: Leukokoria in the first months or years of life. Funnel-shaped, excavation of the optic disc and peripapillary retina. Enlarged disc with indistinct border surrounded by depigmented areas. White, elevated, hyperplastic glial tissues occupies the central disc. Abnormally narrow, straight vessels radiated from the disc margins E-Mail Address. Password. Forgotten Password? Remember M Retinal detachment in morning glory syndrome treated by triamcinolone acetonide-assisted pars plana vitrectomy Hiroyoshi Matsumoto, Hiroshi Enaida, Toshio Hisatomi, Akifumi Ueno, Takao Nakamura, Ichiro Yamanaka, Taiji Sakamoto, Tatsuro Ishibash

Treatment of Total Retinal Detachment in Morning Glory

Optic disc excavations include Optic disc coloboma, Morning Glory Syndrome (MGS), Peripapillary staphyloma and Optic disc pit. We describe A case of a 70 year old lady with MGS, and the role of 3D Optical coherence tomography (OCT) in the management of MGS. Keywords: morning glory syndrome, optical computerized tomography, retinal detachment Morning Glory Syndrome. Show Description + Posted: 10/04/2016. Keywords: 2015 • ASRS • Austria • detachment • morning glory • RD • Retinal Detachment. Figure 2.111. Walker-Warburg syndrome is an autosomal recessive disorder with absence of the normal cascade of retinal differentiation reflected in abnormal development of all retinal layers. Remnant retina is retrolental (behind the lens) and lissencephaly is present in the central nervous system. 2.111. 2.113. 2.114. Figure 2.112 Morning glory disc anomaly (MGDA) is most commonly found in white females in childhood with reduced vision. One in two cases have been reported to develop maculopathy or posterior pole retinal detachment as they grow older. The pathophysiology of MGDA-associated maculopathy is not well understood. We describe a 31-year-old black woman, who presented with gradual reduction of vision in the. Discussion: Morning Glory Syndrome is an uncommon congenital disorder characterized by a widely enlarged papilla, pink-orange in color, with a small glial tuft in the center. The retinal vessels are arranged radially in relation to th

Ocular associations found in affected eyes with morning glory disc anomaly may include retinal detachment, congeni-tal cataract, persistent hyaloid remnants, lid haemangioma and preretinal gliosis [1]. Retinal detachment is the most common ocular complication. . The posterior lenticonus ha A 31-year-old woman with morning glory optic disc anomaly (MGDA) developed acute retrobulbar optic neuritis and a bullous macular detachment. MRI demonstrated truncation of the perineural space of the affected optic nerve as well as focal optic nerve enhancement 13. Irvine AR, Crawford JB, Sullivan JH. The pathogenesis of retinal detachment with morning glory disc and optic pit. Retina. 1986;6(3):146-150. 14. Sugar HS. An explanation for the acquired macular pathology associated with congenital pits of the optic disc. Am J Ophthalmol. 1964;57:833-835. 15. Jain N, Johnson MW Morning glory disc anomaly (MGDA), also known as morning glory syndrome, is a rare congenital malformation of the optic nerve which is frequently associated with midline abnormalities of the brain and skull 1. Epidemiology Morning glory disc an..

Morning glory syndrome Genetic and Rare Diseases

  1. Fei P, Zhang Q, Li J, Zhao P. Clinical characteristics and treatment of 22 eyes of morning glory syndrome associated with persistent hyperplastic primary vitreous. Br J Ophthalmol . 2013 ; 97 (10):1262-1267. 10.1136/bjophthalmol-2013-30356
  2. Chang S, Haik BG, Ellsworth RM, St Louis L, Berrocal JA (1984) Treatment of total retinal detachment in morning glory syndrome. Am J Ophthalmol 97:596-600. CAS PubMed Article Google Scholar 32. Kalina RE, Conrad WC (1976) Intrathecal fluorescein for serous macular detachment. Arch Ophthalmol 94:142
  3. Clinical considerations in complex pediatric cases are far-ranging, from nuanced diagnostic evaluation to ensuring that the parents are prepared. I recently performed surgery on a teenage patient with bilateral morning glory syndrome, retinal detachment, and cataracts
  4. Serous and, less commonly, rhegmatogenous retinal detachment may coexist. 1 Infants with MGDA often manifest strabismus or leukokoria. Morning glory disc anomaly is associated with other midline developmental or vascular malformations. We describe a patient with MGDA and concurrent ipsilateral optic nerve glioma
  5. Morning glory syndrome - optic disc coloboma that may be accompanied by cranial facial, neurologic, and other symptoms; such as glaucoma and retinal detachment. As children with coloboma get older, they may become concerned about the appearance of their eyes. Cosmetic contact lenses can help make the pupil look round rather than keyhole.
  6. Abstract Background The pathogenesis of non-rhegmatogenous retinal detachment (non-RRD) associated with morning glory syndrome (MGS) is not established, as well as best surgical approach to treat RD. Our purpose was to analyse intraoperative optical coherence tomography data (iOCT) in all steps of pars plana vitrectomy (PPV) for non-RRD in MGS.
  7. Such a communication was demonstrated, however, by Chang et al. in an eye with a retinal detachment associated with morning glory anomaly. Irvine and associates ( 32 ) demonstrated communication between the vitreous cavity and the orbit via a morning glory disc anomaly and the subarachnoid space of the optic nerve

The pathogenesis of non-rhegmatogenous retinal detachment (non-RRD) associated with morning glory syndrome (MGS) is not established, as well as best surgical approach to treat RD. Our purpose was to analyse intraoperative optical coherence tomography data (iOCT) in all steps of pars plana vitrectomy (PPV) for non-RRD in MGS, in order to follow pathophysiological aspects of the disease and to. RETINAL DETACHMENT The detachment produces a bright continuous, folded appearance with insertion into the disc and ora serrata. It is to determine the configuration of the detachment as shallow, flat or bullous 51. EXUDATIVE RETINAL DETACHMENT 52. RHEGMATOGENOUS RD 53. RHEGMATOGENOUS RETINAL DETACHMENT 54

Rhegmatogenous Detachment. The most commonly seen retinal detachment. Usually there is/are retinal break (s) induced by posterior vitreous detachment. Fluid from liquefied vitreous can pass through the break (s), enter the potential subretinal space and undermine the retina from the RPE BACKGROUND: The pathogenesis of non-rhegmatogenous retinal detachment (non-RRD) associated with morning glory syndrome (MGS) is not established, as well as best surgical approach to treat RD. Our purpose was to analyse intraoperative optical coherence tomography data (iOCT) in all steps of pars plana vitrectomy (PPV) for non-RRD in MGS, in order to follow pathophysiological aspects of the. Retinal detachment - classification, Lattice degeneration, retinal pigment epithelial detachment. Management Urgent. A retinal detachment in which the macula is not yet involved is an ocular emergency needing treatment within 24 hours. If the macular has already detached, then treatment is still urgent, 48-96 hours. Morning Glory Syndrome.

Morning Glory Syndrome. American Academy of Ophthalmology. October 14, -Shahrezaei S & Binder S. Intraoperative optical coherence tomography assisted analysis of pars Plana vitrectomy for retinal detachment in morning glory syndrome: a case report. BMC Ophthalmology. 2017; 17:134 Chang S, Gregory-Roberts E, Chen R. Retinal detachment associated with optic disc colobomas and morning glory syndrome. Eye (Lond). 2012;26(4):494-500. Müller B, Joussen AM. Myopic traction maculopathy - vitreoretinal traction syndrome in high myopic eyes and posterior staphyloma. Klin Monbl Augenheilkd. 2011;228(9):771-9 Optic nerve anomalies, including optic pit and morning glory disc Inflammatory and infectious diseases affecting the retina and choroid in children Neovascularization of the retina and choroid, as in sickle cell disease/trait, juvenile-onset diabetes, Eales disease, etc

Aicardi syndrome (AS) is a triad of features: agenesis of corpus collosum, chorioretinal lacunae, and infantile spasms. The etiology of Aicardi syndrome is unknown; however, the disorder is almost always seen in females and is thought to be a de novo mutation on the X-chromosome with hemizygous lethality in males. 1 There are reports of males. The morning glory disc anomaly named because it closely resembles the morning glory flower. There is also a geyser in Yellowstone called Morning Glory for the same reason. The characteristic feature of the morning glory disc anomaly is the abnormally straight retinal vessels that emanate from the disc margin (rather than from a central vessel)

Morning Glory Disc Anomaly in Association With IpsilateralMorning Glory Disc - Retina Image Bank3

The findings were compatible with a bilateral morning-glory syndrome, with macular involvement, presenting with a unilateral retinal detachment, prompting urgent surgery. 3 years later, the patient returned with complaints of loss of vision in the right eye, which also presented with a retinal detachment requiring surgical intervention Representative OCT shows retinal pigment epithelium lining an excavation surrounding the optic nerve, characteristic of morning glory syndrome. Comment Morning glory disc anomaly is a congenital anomaly of the optic disc that is typically unilateral (for review see Brodsky 1 )

Postoperative follow-up of a case of atypical morning

Retinal Detachment Surgery in Morning Glory Syndrome - Eyetub

  1. The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: It may also be responsible for a retinal dystrophy. Knobloch 2 syndrome was identified in a single female born to consanguineous parents. It has been argued that the morning glory disc anomaly may be an expression of this syndrome but this remains to be established
  2. ation was performed and the patient underwent a pars plana vitrectomy of the left eye
  3. In the papillorenal syndrome, the hereditary absence of the central retinal vessels may be missed, leading to confusion with isolated optic nerve coloboma, low-tension glaucoma, and morning glory anomaly
  4. DISCUSSION • Morning Glory disc is defined as an enlarged disc with a funnel shaped excavated peri-papillary region that is surrounded by a wide elevated annulus of chorioretinal pigment, with a central white tissue and retinal vessels that exit at the edge of the disc and run radially towards the peripheral fundus.1 • Etiology - poorly.
  5. The 'morning glory syndrome' - a mesodermal defect? Journal Article (Journal Article) The clinical, ultrasonographic, CAT scan and pathologic findings are described in a case of a rare unilateral malformation involving the optic disc of the type described as the 'morning glory syndrome'

Retinal Detachment in Morning Glory Syndrome Treated by

Search the Retina Atlas. keywords / disease type / diagnostics / syndrome. The world's first evolving online retina resource written and reviewed by ASRS members. More ». Anatomy, Structure and Function. Diagnostic Testing. Inflammatory Disease of Vitreous Retina and Choroid. Laser Progressive macular dystophy, central retinal atrophy, macular flecks, later disease onset and scattered flecks with Fundus Flavimaculatus: AD, AR: ABCA4 (majority cases), ELOVL4, PROM1 #248200, #600110, #603786 STICKLER SYNDROME: Myopia, retinal detachment, cataracts, glaucoma, vitreoretinal degeneration, no ocular signs (type III Ho C L, Wei L C. Rhegmatogenous retinal detachment in morning glory syndrome pathogenesis and treatment. Int Ophthalmol, 2001,24(1):21-24. PubMed Article CAS Google Scholar 8. Handmann M. Erbliche Vermutlich angeborene Ientralgefaesse. Klin Monatsbl Augeaheikd, 1929,83:145. Google Scholar So-called morning glory syndrome (MGS), although first described in 1929, owes its name to Kindler (1970). 1 In this syndrome, congenital optic nerve dysplasia exists. The incidence of MGS is very low, and it is caused by the failure of the closure of the choroidal embryonic fissure

Lattice Degeneration - Vitreoretinal Research Group

Description. Morning glory syndrome (MGS) is an optic neuropathy characterized by a congenital funnel shaped excavation of the posterior fundus that incorporates the optic disc malformation (resembling the morning glory flower) MGS is usually unilateral and may result in a decrease in best-corrected visual acuity (BCVA) Abstract: The clinical features of the morning glory syndrome (MSG) are demonstrated in a 12-year-old male patient with the posterior lenticonus in the left eye. This patient had retinal detachment in the left eye. A complete ocular examination was performed and the patient underwent a pars plana vitrectomy of the left eye I. Algorithms Recurrent Corneal Erosion Syndrome 35 Retinal Detachment 36 Acute Conjunctivitis Retinal Hemorrhage 37 Vascular 506 Moebius Syndrome 428 Paget's Disease 508 Morning Glory Syndrome 430 Papilledema 510 Multifocal Choroiditis/Punctate Inner Choroiditis 432 Papilledema in Children 512 Myasthenia Gravis 434 Pattern Dystrophy 514. Morning glory syndrome: A birth defect of the optic nerve (the nerve to the eye) in which there is a coloboma (cleft) of the optic disc.The coloboma results in a funnel-shaped optic nerve head with a white dot in the center, an elevated ring of pigment around the disk, and vessels radiating out from the ring like spokes. Reflection from within the eye may give the appearance of a white pupil

Retinal Detachment in The Morning Glory Syndrome

Other developmental disorders, such as optic nerve colobomas, morning glory disc, and optic nerve pits, are associated with a combination of retinoschisis and serous detachment of the neural retina.[16] [17] For shallow detachments, demarcating laser treatment can be effective, whereas for larger detachments vitrectomy and gas tamponade may be. Retinal vessels are anomalous as well. They are often increased in number and have a generally straight course in the peripapillary region. It has been argued that the morning glory disc anomaly may be an expression of this syndrome but this remains to be established The morning glory disc anomaly (MGDA) is a congenital deformity resulting from failure of the optic nerve to completely form in utero. The term was coined in 1970 by Kindler, noting a resemblance of the malformed optic nerve to the morning glory flower. The condition is usually unilateral Cennamo G, Sammartino A, Fioretti F (1983) Morning glory syndrome with contractile peripapillary staphyloma. Br J Ophthalmol 67: 346-348. Google Scholar 8. Chang S, Haik BG, Ellsworth RM, St. Louis L (1984) Treatment of total retinal detachment in morning glory syndrome. Am J Ophthalmol 97: 596-600. Google Schola Figure 132-10 Morning glory optic disc in this left eye is associated with a shallow retinal detachment. The yellow pigment that overlies the area of subretinal fibrosis at the 3 o'clock position is due to the xanthophyll pigment in the fovea, which is abnormally close to the disc

Review-Ophthalmology (retina): Oral Boards Differential diagnosis. Associated with VHL on ch 3 can get cerebral hemangioblastomas, pancreatic, kidney, and liver. Renal cell carcinoma and pheochromocytoma also. Optic pit, macular detachment secondary to rhegmatogenous retinal detachment, and pigment epithelial detachment (ARMD) Treatment of total retinal detachment in morning glory syndrome. (medscape.com) Prevent Retinal Detachment 1. The best way to prevent retinal detachment is to wear protective eyewear and see your eye doctor in case of injury. (hutchinsonsurgery.com) Occurs when the retina 1 Morning glory syndrome and its many associated ocular anomalies have been reported previously . In a histopathologic study, a case of MGS with many other anomalies including PHPV, Peters anomaly, congenital cataract, total retinal detachment,.

Discover images - Retina Image BankRetinal Detachment | Columbia Ophthalmology

Recognizing Pathology. This material is designed as a searchable reference resource to support clinical decision making. The information contained here should be used as a general guidance when viewing opto map images. The differential diagnosis should be made under the direction of the responsible physician Morning Glory 1. Glaucoma 2. Coloboma 3. Morning Glory 4. Posterior Retinal Detachment 4. Trauma CRVO - Central Retinal Vein Occlusion 1. CRAO 2. CRVO 3. Retinal Detachment 4. Trauma Floppy Iris Syndrome 3. Retinal Detachment •3/23/2016 •10 Cataract 1. Dense Congenital Cataract 2. Traumatic Cataract - Soccer Bal Renal coloboma syndrome (RCS), also called papillorenal syndrome, is an autosomal dominant condition characterized by optic nerve dysplasia and renal hypodysplasia. The eye anomalies consist of a wide and sometimes excavated dysplastic optic disc with the emergence of the retinal vessels from the periphery of the disc, frequently called optic. Coloboma of optic nerve, is a rare defect of the optic nerve that causes moderate to severe visual field defects.. Coloboma of the optic nerve is a congenital anomaly of the optic disc in which there is a defect of the inferior aspect of the optic nerve. The issue stems from incomplete closure of the embryonic fissure while in utero. A varying amount of glial tissue typically fills the defect.

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