Dental anomalies in Axenfeld-Rieger syndrome

International Journal of Paediatric Dentistry

Volumn 15, Issue 6, 2005, Pages 459-463

  O'Dwyer, E M ^a   Jones, D C ^a  

^a ARROWE PARK HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FORKHEAD TRANSCRIPTION FACTOR; FOXC1 PROTEIN, HUMAN; HOMEODOMAIN PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR PITX2;

ANTERIOR EYE SEGMENT; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 4; CHROMOSOME 6; CONGENITAL MALFORMATION; DENTAL CARE; DOMINANT GENE; EYE MALFORMATION; FACIES; FEMALE; GENETICS; HUMAN; HYPODONTIA; MULTIPLE MALFORMATION SYNDROME; MUTATION; SYNDROME; TOOTH MALFORMATION;

ABNORMALITIES, MULTIPLE; ANODONTIA; ANTERIOR EYE SEGMENT; CHILD; CHROMOSOMES, HUMAN, PAIR 4; CHROMOSOMES, HUMAN, PAIR 6; DENTAL CARE FOR CHRONICALLY ILL; EYE ABNORMALITIES; FACIES; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GENES, DOMINANT; HOMEODOMAIN PROTEINS; HUMANS; MUTATION; SYNDROME; TOOTH ABNORMALITIES; TRANSCRIPTION FACTORS;

EID: 27644531859     PISSN: 09607439     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-263X.2005.00639.x     Document Type: Article

References (18)

1. Shields MB, Buckley E, Klintworth GK, Thresher R. Axenfeld-Rieger syndrome. A spectrum of developmental disorders. Survey of Ophthalmology 1985; 29: 387.
2. Wesley RK, Golnick AL. Rieger's Syndrome. Journal of Pediatric Ophthalmology and Strabismus 1978; 15 (2): 67-70.
3. Tabbara KF, Khouri FP, Der Kaloustian V. Rieger's Syndrome with chromosomal anomaly. Canadian Journal of Ophthalmology 1973; 8: 488-490.
4. Gorlin R, Pindborg J, Cohen M. Rieger's syndrome. In: Gorlin R, Pindborg J, Cohen M. (eds). Syndromes of the Head and Neck, 2nd edn. New York, NY: McGraw-Hill, 1976: 649-651.
5. Riekman G. Rieger's syndrome: case report. Canadian Journal of Dentistry for Children 1981; 48 (1): 55-56.
6. Grosso S, Farnetani MA, Berardi R, et al. Familial Axenfeld-Rieger Anomaly, cardiac malformations and sensorineural hearing loss: a provisionally unique genetic syndrome? American Journal of Medical Genetics 2002; 111: 182-186.
7. Jorgenson RJ, Stefan Levin L, Cross HE, Yoder F, Kelly TE. The Rieger Syndrome. American Journal of Medical Genetics 1978; 2: 307-318.
8. Fitch N, Kabach M. The Axenfeld Syndrome and the Rieger Syndrome. The Journal of Medical Genetics 1978; 15: 30-34.
9. Lapeer G. Rieger's Syndrome, severe dental anomalies with mild ophthalmic changes - a case report. Journal of the Canadian Dental Association 1986; 11: 935-937.
10. Dimitrakopoulos J, Voyatzis N, Katopodi T. Rieger syndrome: a case report. Journal of Oral and Maxillofacial Surgery 1997; 55: 517-521.
11. Heckenlively JR, Istenburg SJ, Fox LE. The Rieger Syndrome: a heritable disorder associated with glaucoma. The Johns Hopkins Medical Journal 1982; 151 (6): 351-355.
12. Childers NK, Wright JT. Dental and craniofacial anomalies of Axenfeld-Rieger syndrome. Journal of Oral Pathology 1986; 15: 534-539.
13. Prabhu NT, John R, Munshi AK. Rieger's syndrome: a case report. Quintessence International 1997; 28: 749-752.
14. Scarparo Caldo-Teixera A, Puppin-Rontani RM. Management of severe partial hypodontia: case report. Journal of Clinical Pediatric Dentistry 2003; 27 (2): 133-136.
15. Ozekis H, Shirai S, Ikeda K, Ogura Y. Anomalies associated with Axenfeld-Rieger syndrome. Graese's Archive for Clinical and Experimental Ophthalmology 1999; 237 (9): 730-734.
16. Vaux C, Sheffield L, Gregory Keith C, Voullaire L. Evidence that Rieger syndrome maps to 4q25 or 4q27. Journal of Medical Genetics 1992; 29: 256-258.
17. Priston M, Kozlowski K, Gill D, et al. Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome. Human Molecular Genetics 2001; 10 (16): 1631-1638.
18. Epinoza HM, Cox CJ, Semina EV, Amendit BA. A molecular basis for differential developmental deformities in Axenfeld-Rieger's syndrome. Human Molecular Genetics 2002; 11 (7): 743-753.