Unilateral Peters' anomaly in a patient with DiGeorge syndrome

Journal of Pediatric Ophthalmology and Strabismus

Volumn 42, Issue 5, 2005, Pages 311-313

  Casteels, I ^a,b   Devriendt, K ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b Department of Ophthalmology ^*  (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

AMBLYOPIA; ARTICLE; BIOMICROSCOPY; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CORNEA DISEASE; CORNEA OPACITY; DIGEORGE SYNDROME; EYELID CLOSURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INFANT; NEURAL CREST; OPHTHALMOLOGY; OPHTHALMOSCOPY; PETERS ANOMALY; RETINOSCOPY;

EID: 25644454373     PISSN: 01913913     EISSN: None     Source Type: Journal    
DOI: 10.3928/0191-3913-20050901-17     Document Type: Article

References (13)

1. Perez E, Sullivan KE. Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes). Curr Opin Pediatr 2002;14:678-683.
2. Shprintzen RJ, Goldberg RB, Lewin ML, et al. A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome. Cleft Palate J 1978;15:56-62.
3. Mansour AM, Goldberg RB, Wang FM, Shprintzen RJ. Ocular findings in the velo-cardio-facial syndrome. J Pediatr Ophthalmol Strabismus 1987;24:263-266.
4. Motzin B, Marion R, Goldberg R, et al. Variable phenotypes in velocardiofacial syndrome with chromosomal deletion. J Pediatr 1993;123:406-410.
5. Beemer FA, de Nef JJEM, Delleman JW, et al. Additional eye findings in a case of velo-cardio-facial syndrome. Am J Med Genet 1986;24:541-542.
6. Fitch N. Velo-cardio-facial syndrome and eye abnormality. Am J Med Genet 1983;15:669.
7. Etchevers HC, Vincent C, Le Douarin NM, et al. The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain. Development 2001;128:1059-1068.
8. Devriendt K, Swillen A, Fryns JP. Deletion in chromosome 22q11 in a child with CHARGE association. Clin Genet 1998;53:408-410.
9. Digilio MC, Giannotti A, Marino B, et al. Radial aplasia and chromosome 22q11 deletion. J Med Genet 1997;34:942-944.
10. Johnston MC, Bhakdinaronk A, Reid YC. An expanded role of the neural crest in oral and pharyngeal development. In: Bosma JD, ed. Fourth Symposium on Oral Sensation and Perception: Development in the Fetus and Infant. Washington, DC: U.S. Government Printing Office; 1974:37-52.
11. Kenyon KR. Mesenchymal dysgenesis in Peter's anomaly, sclerocornea and congenital endothelial dystrophy. Exp Eye Res 1975;21:125-142.
12. Kupfer C, Kaiser-Kupfer MI. New hypothesis of developmental anomalies of the anterior chamber associated with glaucoma. Transactions of the Ophthalmological Societies of the United Kingdom 1978;98:213-215.
13. Bahn CF, Falls HF, Varley GA, et al. Classification of corneal endothelial disorders based on neural crest origin. Ophthalmology 1984;91:558-563.