« Previous
Next »
Contact Lens & Anterior Eye
Volume 33, Issue 1
, Pages 41-42
, February 2010
Keratoconus associated with the Pierre Robin Sequence
References
- . Keratoconus. Surv Ophthalmol. 1998;42:297–319
- VSZ1: a gene for posterior polymorphous dystrophy and keratoconus. Hum Mol Genet. 2002;11:1029–1036
- VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation. Invest Ophthalmol Vis Sci. 2005;46:39–45
- . Backward fall of the root of the tongue as a cause of respiratory disturbances. Bull Acad Med (Paris). 1923;89:37
- . Diagnosis and treatment of the Pierre Robin sequence: results of a retrospective clinical study and review of the literature. Eur J Pediatr. 2001;160:47–53
- . Robin sequences and complexes: causal heterogeneity and pathogenetic/phenotypic variability. Am J Med Genet. 1999;84:311–315
- Visual complications of Stickler syndrome in paediatric patients with Robin sequence. J Craniomaxillofac Surg. 2007;35:76–80
- . Aicardi syndrome with Pierre Robin sequence. J AAPOS. 2004;8:187–189
- Congenital alacrima in Pierre Robin sequence. Cornea. 2004;23:632–634
- . Pierre Robin sequence with unilateral anophthalmia and lower limb oligodactyly: an unusual presentation of ophthalmoacromelic syndrome?. Clin Dysmorphol. 2008;17:187–188
PII: S1367-0484(09)00126-X
doi: 10.1016/j.clae.2009.09.003
© 2009 British Contact Lens Association. Published by Elsevier Inc. All rights reserved.
« Previous
Next »
Contact Lens & Anterior Eye
Volume 33, Issue 1
, Pages 41-42
, February 2010
