منابع مشابه
Primary gelatinous drop-like keratopathy.
This paper describes three siblings, the only affected members of the family, with gelatinous drop-like keratopathy. This rare form of primary corneal amyloidosis has been reported almost exclusively in Japanese literature, and to our knowledge this is the first report of the condition seen in the United Kingdom. Clinical and histological details are presented. The nature and possible aetiology...
متن کاملLimbal Stem Cell Transplantation for Gelatinous Drop-like Corneal Dystrophy
PURPOSE To report the outcomes of allograft limbal stem cell transplantation for recurrent gelatinous drop-like corneal dystrophy (GDLD). METHODS In this non-comparative interventional case series, 4 eyes of 3 consecutive patients with recurrent GDLD underwent allograft limbal stem cell transplantation. Two eyes underwent concomitant penetrating keratoplasty while the other two underwent simu...
متن کاملNovel Mutations in TACSTD2 Gene in Families with Gelatinous Drop-like Corneal Dystrophy (GDLD)
In the current study, we conducted a mutation screening of tumor-associated calcium signal transducer 2 (TACSTD2) gene in six consanguineous Iranian families with gelatinous drop-like corneal dystrophy (GDLD), in order to find the causative mutations. Detailed eye examination was performed by ophthalmologist to confirm GDLD in patients. To detect the possible mutations, direct Sanger sequencing...
متن کاملA novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy
PURPOSE To identify the molecular defect causing gelatinous drop-like corneal dystrophy (GDLD) in two Chinese brothers and report the morphological evaluation of GDLD by laser scanning confocal microscopy and Fourier-domain optical coherence tomography (OCT). METHODS Genetic analysis included polymerase chain reaction (PCR) amplification and direct nucleotide sequencing of the coding region o...
متن کاملFamilial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin gene.
PURPOSE Because corneal tissue with familial subepithelial corneal amyloidosis (FSCA; gelatinous drop-like dystrophy of the cornea) contains lactoferrin the possibility that the FSCA gene was the human lactoferrin (hLF) gene was investigated. Due to contradictory published information we also mapped the hLF gene. METHODS We mapped the hLF gene using a genomic clone of the entire hLF gene as a...
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ژورنال
عنوان ژورنال: British Journal of Ophthalmology
سال: 1989
ISSN: 0007-1161
DOI: 10.1136/bjo.73.8.661