×
About 225 results

ALLMedicine™ Posterior Polymorphous Corneal Dystrophy Center

Research & Reviews  111 results

Corneal cross-linking for treatment of progressive keratoconus in a patient with Alport...
https://doi.org/10.1177/1120672121997672
European Journal of Ophthalmology; Krolo I, Kasumović A et. al.

Feb 26th, 2021 - Ocular features of Alport syndrome include anterior lenticonus, posterior polymorphous corneal dystrophy, and fleck-and-dot retinopathy in most cases. Keratoconus in such patients has been rarely mentioned in previous studies. To our knowledge, th...

Laser refractive surgery in corneal dystrophies.
https://doi.org/10.1097/j.jcrs.0000000000000468
Journal of Cataract and Refractive Surgery; Rocha-de-Lossada C, Rachwani-Anil R et. al.

Nov 5th, 2020 - Twenty-eight case reports and case series published between 2000 and 2019 concerning laser refractive surgery in patients with corneal dystrophies, resulting in 173 eyes from 94 patients, were included in this systematic review. Best results were ...

CUGC for posterior polymorphous corneal dystrophy (PPCD).
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906511
European Journal of Human Genetics : EJHG; Davidson AE, Hafford-Tear NJ et. al.

Jun 15th, 2019 - Name of the disease (synonyms) CUGC for posterior polymorphous corneal dystrophy (PPCD).OMIM# of the disease 122000; 609141; 618031.Name of the analysed genes or DNA/chromosome segments OVOL2 (PPCD1); ZEB1 (PPCD3); GRHL2 (PPCD4).OMIM# of the gene(...

ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellula...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6564028
PloS One; Frausto RF, Chung DD et. al.

Jun 13th, 2019 - The zinc finger e-box binding homeobox 1 (ZEB1) transcription factor is a master regulator of the epithelial to mesenchymal transition (EMT), and of the reverse mesenchymal to epithelial transition (MET) processes. ZEB1 plays an integral role in m...

see more →

Clinicaltrials.gov  113 results

Corneal cross-linking for treatment of progressive keratoconus in a patient with Alport...
https://doi.org/10.1177/1120672121997672
European Journal of Ophthalmology; Krolo I, Kasumović A et. al.

Feb 26th, 2021 - Ocular features of Alport syndrome include anterior lenticonus, posterior polymorphous corneal dystrophy, and fleck-and-dot retinopathy in most cases. Keratoconus in such patients has been rarely mentioned in previous studies. To our knowledge, th...

Laser refractive surgery in corneal dystrophies.
https://doi.org/10.1097/j.jcrs.0000000000000468
Journal of Cataract and Refractive Surgery; Rocha-de-Lossada C, Rachwani-Anil R et. al.

Nov 5th, 2020 - Twenty-eight case reports and case series published between 2000 and 2019 concerning laser refractive surgery in patients with corneal dystrophies, resulting in 173 eyes from 94 patients, were included in this systematic review. Best results were ...

CUGC for posterior polymorphous corneal dystrophy (PPCD).
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906511
European Journal of Human Genetics : EJHG; Davidson AE, Hafford-Tear NJ et. al.

Jun 15th, 2019 - Name of the disease (synonyms) CUGC for posterior polymorphous corneal dystrophy (PPCD).OMIM# of the disease 122000; 609141; 618031.Name of the analysed genes or DNA/chromosome segments OVOL2 (PPCD1); ZEB1 (PPCD3); GRHL2 (PPCD4).OMIM# of the gene(...

ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellula...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6564028
PloS One; Frausto RF, Chung DD et. al.

Jun 13th, 2019 - The zinc finger e-box binding homeobox 1 (ZEB1) transcription factor is a master regulator of the epithelial to mesenchymal transition (EMT), and of the reverse mesenchymal to epithelial transition (MET) processes. ZEB1 plays an integral role in m...

see more →

News  1 results

Unilateral Glaucoma?
https://www.medscape.com/viewarticle/859213_2

Feb 24th, 2016 - Case Diagnosis The correct diagnosis is iridocorneal endothelial (ICE) syndrome. ICE syndrome should be in the differential diagnosis for any young to middle-aged adult who presents with an acquired unilateral disorder associated with iris anomali...

see more →