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About 177 results

ALLMedicine™ Lattice Corneal Dystrophy Center

Research & Reviews  87 results

A novel missense TGFBI variant p.(Ser591Phe) in a Finnish family with variant lattice c...
https://doi.org/10.1177/1120672121997305
European Journal of Ophthalmology; Jaakkola AM, Järventausta PJ et. al.

Mar 1st, 2021 - We describe the phenotype of a variant lattice corneal dystrophy (LCD) potentially caused by a novel variant c.1772C>T p.(Ser591Phe) in exon 13 of the transforming growth factor beta-induced (TGFBI) gene. The proband, a 71-year-old woman referred ...

Coexistence of Meesmann Corneal Dystrophy and a Pseudo-Unilateral Lattice Corneal Dystr...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861493
Cornea Abad-Morales V, Barbany M et. al.

Dec 21st, 2020 - This study aims to clinically and genetically report a case of coexisting Meesmann corneal dystrophy (MECD) and pseudo-unilateral lattice corneal dystrophy (LCD). Clinical characterization was supported by a complete ophthalmological evaluation, i...

Contact lens induced bacterial keratitis in LCD II: Management and multimodal imaging: ...
https://doi.org/10.1177/1120672120968724
European Journal of Ophthalmology; Alafaleq M, Knoeri J et. al.

Oct 30th, 2020 - To describe the management and multimodal imaging of lattice corneal dystrophy type II (LCD-II) complicated by an infectious keratitis due to a bandage contact lens and to review current literature. A 50-year-old female was diagnosed with Meretoja...

Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with fa...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195602
Molecular Vision; Cabral-Macias J, Garcia-Montaño LA et. al.

May 5th, 2020 - Familial amyloidosis of the Finnish type (FAF) is an inherited amyloidosis arising from mutations in the gelsolin protein (GSN). The disease includes facial paralysis, loose skin, and lattice corneal dystrophy. To date, FAF has been invariably ass...

Association of unilateral lattice corneal dystrophy on slit lamp and bilateral confocal...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002701
Eye (London, England); De Sousa Peixoto R, Mutch S et. al.

Jul 4th, 2019 - Association of unilateral lattice corneal dystrophy on slit lamp and bilateral confocal microscopy features with H572R mutation in the TGFBI gene.|2019|De Sousa Peixoto R,Mutch S,Eason J,Jaakson K,Haamer E,|pathology,diagnosis,genetics,metabolism,...

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Clinicaltrials.gov  89 results

A novel missense TGFBI variant p.(Ser591Phe) in a Finnish family with variant lattice c...
https://doi.org/10.1177/1120672121997305
European Journal of Ophthalmology; Jaakkola AM, Järventausta PJ et. al.

Mar 1st, 2021 - We describe the phenotype of a variant lattice corneal dystrophy (LCD) potentially caused by a novel variant c.1772C>T p.(Ser591Phe) in exon 13 of the transforming growth factor beta-induced (TGFBI) gene. The proband, a 71-year-old woman referred ...

Coexistence of Meesmann Corneal Dystrophy and a Pseudo-Unilateral Lattice Corneal Dystr...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861493
Cornea Abad-Morales V, Barbany M et. al.

Dec 21st, 2020 - This study aims to clinically and genetically report a case of coexisting Meesmann corneal dystrophy (MECD) and pseudo-unilateral lattice corneal dystrophy (LCD). Clinical characterization was supported by a complete ophthalmological evaluation, i...

Contact lens induced bacterial keratitis in LCD II: Management and multimodal imaging: ...
https://doi.org/10.1177/1120672120968724
European Journal of Ophthalmology; Alafaleq M, Knoeri J et. al.

Oct 30th, 2020 - To describe the management and multimodal imaging of lattice corneal dystrophy type II (LCD-II) complicated by an infectious keratitis due to a bandage contact lens and to review current literature. A 50-year-old female was diagnosed with Meretoja...

Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with fa...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195602
Molecular Vision; Cabral-Macias J, Garcia-Montaño LA et. al.

May 5th, 2020 - Familial amyloidosis of the Finnish type (FAF) is an inherited amyloidosis arising from mutations in the gelsolin protein (GSN). The disease includes facial paralysis, loose skin, and lattice corneal dystrophy. To date, FAF has been invariably ass...

Association of unilateral lattice corneal dystrophy on slit lamp and bilateral confocal...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002701
Eye (London, England); De Sousa Peixoto R, Mutch S et. al.

Jul 4th, 2019 - Association of unilateral lattice corneal dystrophy on slit lamp and bilateral confocal microscopy features with H572R mutation in the TGFBI gene.|2019|De Sousa Peixoto R,Mutch S,Eason J,Jaakson K,Haamer E,|pathology,diagnosis,genetics,metabolism,...

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News  1 results

Horizontal Diplopia at Distance and Right Gaze
https://www.medscape.com/viewarticle/865025_3

Jun 22nd, 2016 - Discussion An amyloidoma is an extracellular aggregation of misfolded insoluble proteins and is considered a monoclonal immunoglobulin deposition disease.[1] Approximately 20 unrelated proteins are known to form amyloid fibrils in vivo; each is as...

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