Dystrophy

Variant lattice corneal dystrophy associated with compound heterozygous mutations in the TGFBI gene
Lydia Bai-Tsin Ann, Alessandro Abbouda, Ricardo F Frausto, Samira Huseynli, Kishan Gupta, Jorge L Alió, Anthony J Aldave

British Journal of Ophthalmology Apr 2017, 101 (4) 509-513; DOI: 10.1136/bjophthalmol-2015-307602
Gelatinous drop-like corneal dystrophy: a review
Hrishikesh Kaza, Manas R Barik, Mamatha M Reddy, Ruchi Mittal, Sujata Das

British Journal of Ophthalmology Jan 2017, 101 (1) 10-15; DOI: 10.1136/bjophthalmol-2016-309555
Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options
Preena Tanna, Rupert W Strauss, Kaoru Fujinami, Michel Michaelides

British Journal of Ophthalmology Jan 2017, 101 (1) 25-30; DOI: 10.1136/bjophthalmol-2016-308823
Preserved visual function in retinal dystrophy due to hypomorphic RPE65 mutations
Sarah Hull, Graham E Holder, Anthony G Robson, Rajarshi Mukherjee, Michel Michaelides, Andrew R Webster, Anthony T Moore

British Journal of Ophthalmology Nov 2016, 100 (11) 1499-1505; DOI: 10.1136/bjophthalmol-2015-308019
RPGR-associated retinopathy: clinical features, molecular genetics, animal models and therapeutic options
James J L Tee, Alexander J Smith, Alison J Hardcastle, Michel Michaelides

British Journal of Ophthalmology Aug 2016, 100 (8) 1022-1027; DOI: 10.1136/bjophthalmol-2015-307698
Assessment of estimated retinal atrophy progression in Stargardt macular dystrophy using spectral-domain optical coherence tomography
Rupert W Strauss, Beatriz Muñoz, Yulia Wolfson, Raafay Sophie, Emily Fletcher, Millena G Bittencourt, Hendrik P N Scholl

British Journal of Ophthalmology Jul 2016, 100 (7) 956-962; DOI: 10.1136/bjophthalmol-2015-307035
Novel morphological macular findings in juvenile CLN3 disease
S Dulz, L Wagenfeld, M Nickel, G Richard, R Schwartz, U Bartsch, A Kohlschütter, A Schulz

British Journal of Ophthalmology Jun 2016, 100 (6) 824-828; DOI: 10.1136/bjophthalmol-2015-307320
The ophthalmic phenotype of IFT140-related ciliopathy ranges from isolated to syndromic congenital retinal dystrophy
Inam N Bifari, Sahar M Elkhamary, Hanno J Bolz, Arif O Khan

British Journal of Ophthalmology Jun 2016, 100 (6) 829-833; DOI: 10.1136/bjophthalmol-2015-307555
C21orf2 is mutated in recessive early-onset retinal dystrophy with macular staphyloma and encodes a protein that localises to the photoreceptor primary cilium
Arif O Khan, Tobias Eisenberger, Kerstin Nagel-Wolfrum, Uwe Wolfrum, Hanno J Bolz

British Journal of Ophthalmology Dec 2015, 99 (12) 1725-1731; DOI: 10.1136/bjophthalmol-2015-307277
Comparison of primary graft survival following penetrating keratoplasty and Descemet's stripping endothelial keratoplasty in eyes with prior trabeculectomy
Shawn M Iverson, Oriel Spierer, George C Papachristou, William J Feuer, Wei Shi, David S Greenfield, Terrence P O'Brien

British Journal of Ophthalmology Nov 2015, 99 (11) 1477-1482; DOI: 10.1136/bjophthalmol-2014-306547

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