127 related articles for article (PubMed ID: 2594319)
1. The Rieger anomaly concomitant with multiple dental, craniofacial, and somatic midline anomalies and short stature.
Brooks JK; Coccaro PJ; Zarbin MA
Oral Surg Oral Med Oral Pathol; 1989 Dec; 68(6):717-24. PubMed ID: 2594319
[TBL] [Abstract][Full Text] [Related]
2. Dental and craniofacial anomalies of Axenfeld-Rieger syndrome.
Childers NK; Wright JT
J Oral Pathol; 1986 Nov; 15(10):534-9. PubMed ID: 3104560
[TBL] [Abstract][Full Text] [Related]
3. Axenfeld-Rieger syndrome. A spectrum of developmental disorders.
Shields MB; Buckley E; Klintworth GK; Thresher R
Surv Ophthalmol; 1985; 29(6):387-409. PubMed ID: 3892740
[TBL] [Abstract][Full Text] [Related]
4. Rieger anomaly and uveal coloboma with associated anomalies. Third observation of a rare oculo-palato-osseous syndrome--the Abruzzo-Erikson syndrome.
Verloes A; Dodinval P
Ophthalmic Paediatr Genet; 1990 Mar; 11(1):41-7. PubMed ID: 2348981
[TBL] [Abstract][Full Text] [Related]
5. Axenfeld-Rieger syndrome: report on dental and craniofacial findings.
Jena AK; Kharbanda OP
J Clin Pediatr Dent; 2005; 30(1):83-8. PubMed ID: 16302606
[TBL] [Abstract][Full Text] [Related]
6. The Rieger syndrome: orofacial manifestations. Case report of a rare condition.
Singh J; Pannu K; Lehl G
Quintessence Int; 2003 Oct; 34(9):689-92. PubMed ID: 14982223
[TBL] [Abstract][Full Text] [Related]
7. Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutation.
Meyer-Marcotty P; Weisschuh N; Dressler P; Hartmann J; Stellzig-Eisenhauer A
J Oral Pathol Med; 2008 Sep; 37(8):504-10. PubMed ID: 18331556
[TBL] [Abstract][Full Text] [Related]
8. Anomalies associated with Axenfeld-Rieger syndrome.
Ozeki H; Shirai S; Ikeda K; Ogura Y
Graefes Arch Clin Exp Ophthalmol; 1999 Sep; 237(9):730-4. PubMed ID: 10447647
[TBL] [Abstract][Full Text] [Related]
9. A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene.
Honkanen RA; Nishimura DY; Swiderski RE; Bennett SR; Hong S; Kwon YH; Stone EM; Sheffield VC; Alward WL
Am J Ophthalmol; 2003 Mar; 135(3):368-75. PubMed ID: 12614756
[TBL] [Abstract][Full Text] [Related]
10. A newly recognized syndrome of skeletal dysplasia with opalescent and rootless teeth.
Kantaputra PN
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2001 Sep; 92(3):303-7. PubMed ID: 11552148
[TBL] [Abstract][Full Text] [Related]
11. Axenfeld-Rieger syndrome (ARS): A review and case report.
Waldron JM; McNamara C; Hewson AR; McNamara CM
Spec Care Dentist; 2010; 30(5):218-22. PubMed ID: 20831741
[TBL] [Abstract][Full Text] [Related]
12. KBG syndrome: review of the literature and findings of 5 affected patients.
Kumar H; Prabhu N; Cameron A
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Sep; 108(3):e72-9. PubMed ID: 19716495
[TBL] [Abstract][Full Text] [Related]
13. Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?
Moog U; Bleeker-Wagemakers EM; Crobach P; Vles JS; Schrander-Stumpel CT
Am J Med Genet; 1998 Jul; 78(3):263-6. PubMed ID: 9677063
[TBL] [Abstract][Full Text] [Related]
14. Craniofacial bony defect with developmental abnormality of facial bones, dental malalignment and ectopic neural tissue in the internal auditory meati--a new syndrome?
Colleran GC; Hayes R; Kearns G; Kavanagh P; Moylett E; Lynch SA
Eur J Med Genet; 2014; 57(6):302-5. PubMed ID: 24705061
[TBL] [Abstract][Full Text] [Related]
15. Dental and craniofacial features of Aarskog syndrome: report of a case and review of literature.
Reddy P; Kharbanda OP; Kabra M; Duggal R
J Clin Pediatr Dent; 1999; 23(2):155-9. PubMed ID: 10204459
[TBL] [Abstract][Full Text] [Related]
16. Variability of the cranial and dental phenotype in Williams syndrome.
Axelsson S
Swed Dent J Suppl; 2005; (170):3-67. PubMed ID: 15762376
[TBL] [Abstract][Full Text] [Related]
17. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
[TBL] [Abstract][Full Text] [Related]
18. An unusual case of non-syndromic occurrence of multiple dental anomalies.
Suprabha BS; Sumanth KN; Boaz K; George T
Indian J Dent Res; 2009; 20(3):385-7. PubMed ID: 19884730
[TBL] [Abstract][Full Text] [Related]
19. Newly recognized syndrome of cerebral, ocular, dental, auricular, skeletal anomalies: CODAS syndrome--a case report.
Shebib SM; Reed MH; Shuckett EP; Cross HG; Perry JB; Chudley AE
Am J Med Genet; 1991 Jul; 40(1):88-93. PubMed ID: 1887855
[TBL] [Abstract][Full Text] [Related]
20. Syndrome of Hajdu-Cheney: three case reports of orofacial interest.
Vingerhoedt E; Bailleul-Forestier I; Fellus P; Schoenaers J; Frijns JP; Carels C
Cleft Palate Craniofac J; 2010 Nov; 47(6):645-53. PubMed ID: 20500061
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
