Zobrazeno 1 - 10
of 294
pro vyhledávání: '"Fleischer ring"'
Autor:
Liudmila S. Pateyuk
Publikováno v:
Клиническая практика, Vol 15, Iss 3, Pp 96-108 (2024)
Keratoconus is an ectatic corneal disease, resulting in loss of visual functions in young population. Diagnosis of the disease at a moderate stage with a typical progressive clinical course is not particularly difficult; however, the diagnosis verifi
Externí odkaz:
https://doaj.org/article/05209f35050c4cffa55535ae83d4ad37
Autor:
Monika Korga, Paweł Pawlik, Przemysław Zaroda, Jakub Wawrzkowicz, Patrycja Niewinna, Paweł Dąda, Dominika Mańdziuk, Michał Żuchowski, Klaudia Kołodziej, Wojciech Kołodziej
Publikováno v:
Quality in Sport, Vol 15 (2024)
Wilson's disease, also known as hepatolenticular degeneration, is a rare genetic metabolic disorder that leads to excessive accumulation of copper in the body, particularly in the liver and brain. This results in the gradual damage of these organs an
Externí odkaz:
https://doaj.org/article/babc2924714a4fcbb627b1b074bbf502
Publikováno v:
Current Directions in Biomedical Engineering, Vol 9, Iss 1, Pp 266-269 (2023)
Patients suffering from Wilson’s disease accumulate copper in their body. Copper load may become visible as Kayser-Fleischer (KF) rings - colorful copper-sulfur granules in the base of the cornea. Reoccurrence of KF rings in patients under anti-cop
Externí odkaz:
https://doaj.org/article/b3de010608ab4a63b7a417c3418fcc1b
Autor:
Kalyan Bhattacharya, Bindu Thankappan
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 1, Pp 43-53 (2022)
Wilson's disease (WD) is an autosomal recessive disorder due to ATP7B gene mutation, resulting in defective copper metabolism, with liver and brain being primarily affected. Being a treatable disorder, early diagnosis and proper management of WD may
Externí odkaz:
https://doaj.org/article/91740fa06431426ba53655ad9c338e34
Publikováno v:
GMS Ophthalmology Cases, Vol 13, p Doc08 (2023)
Wilson’s disease, also called hepatolenticular degeneration, has varied clinical manifestations and poses diagnostic challenges. Kayser-Fleischer ring, when present, is considered pathognomic of Wilson’s disease. Although its presence is most com
Externí odkaz:
https://doaj.org/article/1aed0845658a4d8ca26e7d27b7fba953
Autor:
Mehmet Fuat Alakus, Mehtap Caglayan, Nazım Ekin, Hasan Oncul, Esref Arac, Umut Dag, Halit Diri
Publikováno v:
Eye and Vision, Vol 8, Iss 1, Pp 1-8 (2021)
Abstract Background To investigate the topographic measurements and densitometry of corneas in Wilson’s disease (WD) patients with or without a Kayser-Fleischer ring (KF-r) compared to healthy individuals. Methods This cross-sectional study include
Externí odkaz:
https://doaj.org/article/d48a077d94144e649d30add51309ee7d
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 5, Pp 652-663 (2021)
Wilson's disease (WD) is an autosomal recessive disorder due to ATP7B gene mutation, resulting in defective copper metabolism, with the liver and brain being primarily affected. WD being a treatable disorder, early diagnosis and proper management may
Externí odkaz:
https://doaj.org/article/61d0de273be946338168886d64dcd1f9
Publikováno v:
BMC Ophthalmology, Vol 20, Iss 1, Pp 1-4 (2020)
Abstract Background It is rare for hepatolenticular degeneration [Wilson’s disease (WD)] to occur along with keratoconus (KC). In our report, a teenager was diagnosed with WD because of the discovery of Kayser–Fleischer (KF) ring in the cornea, a
Externí odkaz:
https://doaj.org/article/633d86b3ae9740c4ad01a13e1ccf7742
Akademický článek
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Publikováno v:
ScienceRise: Medical Science; № 6 (51) (2022); 25-40
ScienceRise: Medical Science; No. 6 (51) (2022); 25-40
ScienceRise: Medical Science; No. 6 (51) (2022); 25-40
The aims: The purpose of this study was to evaluate and compare the anterior and posterior corneal surface parameters, keratoconus indices, thickness profile data, and data from enhanced elevation maps of keratoconus and normal corneas using Combined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75bff2f95170b8c988ed606e1b0886dc
https://doi.org/10.15587/2519-4798.2022.270264
https://doi.org/10.15587/2519-4798.2022.270264