Morning glory disk anomaly-more than meets the eye

Journal of AAPOS

Volumn 13, Issue 4, 2009, Pages 333-334

  Traboulsi, Elias I ^a  

^a LERNER RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

VISUAL PIGMENT;

CENTRAL NERVOUS SYSTEM; CLINICAL FEATURE; COLOBOMA; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL MALFORMATION; CRANIOFACIAL MALFORMATION; EDITORIAL; GENE EXPRESSION; GENE MUTATION; HUMAN; HYPERTELORISM; HYPOPHYSIS DISEASE; KARYOTYPE 47,XYY; MAGNETIC RESONANCE ANGIOGRAPHY; MORNING GLORY SYNDROME; MOYAMOYA DISEASE; OPTIC DISK ANOMALY; OPTIC NERVE; OPTICAL COHERENCE TOMOGRAPHY; PATHOGENESIS; PRIORITY JOURNAL; RETINA BLOOD VESSEL; Y CHROMOSOME;

EYE ABNORMALITIES; FUNCTIONAL LATERALITY; HUMANS; OPTIC DISK; OPTIC NERVE DISEASES;

EID: 68349101407     PISSN: 10918531     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaapos.2009.05.015     Document Type: Editorial

References (20)

1. Chew F., and Visvaraja S. 47XYY and morning glory syndrome-A unique association. J AAPOS 13 (2009) 406-407
2. Choudhry N., Ramasubramanian A., Shields C.L., Brown G., and Shields J.A. Spontaneous resolution of retinal detachment in morning glory disk anomaly. J AAPOS (2009) In press
3. Loo J.E., Kim K.H., Park H.J., Lee S.J., and Jea S.Y. Morning glory disk anomaly: A computerized analysis of contractile movements with implications for pathogenesis. J AAPOS 13 (2009) 403-405
4. Handman M. Erbliche, vermutlich angeborene zentrale gliose Entartung des Sehnerven mit besonderer Beteiligung der Zentralgefasse. Klin Montasbl Augenheilkd 83 (1929) 145
5. Pedler C. Unusual coloboma of the optic nerve entrance. Br J Ophthalmol 45 (1961) 803-807
6. Kindler P. Morning glory syndrome: Unusual congenital optic disk anomaly. Am J Ophthalmol 69 (1970) 376-384
7. Traboulsi E.I., and O'Neill J.F. The spectrum in the morphology of the so-called "morning glory disc anomaly.". J Pediatr Ophthalmol Strabismus 25 (1988) 93-98
8. Pollock S. The morning glory disc anomaly: Contractile movement, classification, and embryogenesis. Doc Ophthalmol 65 (1987) 439-460
9. Beyer W.B., Quencer R.M., and Osher R.H. Morning glory syndrome: A functional analysis including fluorescein angiography, ultrasonography, and computerized tomography. Ophthalmology 89 (1982) 1362-1367
10. Loddenkemper T., Friedman N.R., Ruggieri P.M., Marcotty A., Sears J., and Traboulsi E.I. Pituitary stalk duplication in association with moya moya disease and bilateral morning glory disc anomaly-Broadening the clinical spectrum of midline defects. J Neurol 255 (2008) 885-890
11. Lee B., and Traboulsi E.I. Morning glory disk anomaly revisited. Ophthalm Genet 29 (2008) 47-52
12. Cook C., Sulik K., and Wright K.W. Embryology. In: Wright K.W., and Spiegel P.H. (Eds). Pediatric Ophthalmology and Strabismus. 2nd ed (2003), Spinger-Verlag, New York 3-38
13. Evans A.L., and Gage P.J. Expression of the homeobox gene Pitx2 in neural crest is required for optic stalk and ocular anterior segment development. Hum Mol Genet 14 (2005) 3347-3359
14. Lenhart P.D., Lambert S.R., Newman N.J., Biousse V., Traboulsi E.I., Hutchinson A.K., et al. Intracranial vascular anomalies in patients with morning glory disk anomaly. Am J Ophthalmol 142 (2006) 644-650
15. Scott R.M., and Smith E.R. Moyamoya disease and moyamoya syndrome. N Engl J Med 360 (2009) 1226-1237
16. Ho T.C., Tsai P.C., Chen M.S., and Lin L.L. Optical coherence tomography in the detection of retinal break and management of retinal detachment in morning glory syndrome. Acta Ophthalmol Scand 84 (2006) 225-227
17. Traboulsi E.I. Morning glory disc anomaly or optic disc coloboma?. Arch Ophthalmol 112 (1994) 153
18. Brodsky M.C. Morning glory disc anomaly or optic disc coloboma?. Arch Ophthalmol 112 (1994) 153
19. Sanyanusin P., McNoe L.A., Sullivan M.J., Weaver R.G., and Eccles M.R. Mutation of PAX2 in two siblings with renal-coloboma syndrome. Hum Mol Genet 4 (1995) 2183-2184
20. Kniestedt C., Landau K., Brodsky M.C., North P., and Waner M. Infantile orofacial hemangioma with ipsilateral peripapillary excavation in girls: A variant of the PHACE syndrome. Arch Ophthalmol 122 (2004) 413-415