Zobrazeno 1 - 10
of 460
pro vyhledávání: '"heterochromia"'
Publikováno v:
Pakistan Journal of Medicine and Dentistry, Vol 13, Iss 4 (2024)
Heterochromia iridis is a rare genetic disorder, characterized by variation in the concentration and distribution of the melanin pigment. It is caused by mutation in genes responsible for the synthesis of melanin pigment iris of the eye. Heterochromi
Externí odkaz:
https://doaj.org/article/e4c66ef1983c442cb6b7b0775488c114
Publikováno v:
Indian Journal of Ophthalmology, Vol 72, Iss 6, Pp 885-889 (2024)
Purpose: To study cases of Fuchs’ uveitis (FU) diagnosed as uveitis other than FU at initial visits. Methods: A retrospective, observational chart review. Details of clinical presentation, initial diagnosis, treatment details, and follow-up before
Externí odkaz:
https://doaj.org/article/e0da1759cdf04b6097208aad21119a8e
Autor:
Hamzeh Mohammad Alrawashdeh
Publikováno v:
Taiwan Journal of Ophthalmology, Vol 14, Iss 1, Pp 125-128 (2024)
Iris mammillations are distinctive uniform nipple-like elevations that cover the anterior surface of the iris partially or totally. It is a rare finding and may coexist with other ocular and extraocular manifestations. Optic nerve pit (ONP), also kno
Externí odkaz:
https://doaj.org/article/63bbd966415948969084071b9e11fd3d
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-6 (2023)
Abstract Background Waardenburg syndrome (WS) is a rare genetic disorder characterized by varying degrees of sensorineural hearing loss and accumulated pigmentation in the skin, hair and iris. The syndrome is classified into four types (WS1, WS2, WS3
Externí odkaz:
https://doaj.org/article/197a71b3e1c04f17b6000c622f603ea9
Autor:
Sijun Li, Mengyao Qin, Shuang Mao, Lingyun Mei, Xinzhang Cai, Yong Feng, Chufeng He, Jian Song
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-14 (2022)
Abstract Background Waardenburg syndrome (WS) is the most common form of syndromic deafness with phenotypic and genetic heterogeneity in the Chinese population. This study aimed to clarify the clinical characteristics and the genetic cause in eight C
Externí odkaz:
https://doaj.org/article/4f5f78041b61473cb8fd3850a8800cf4
Autor:
Fillipe Pedroso-Santos, Jessica Stefany Costa Anaissi, Pedro Henrique Guedes de Lima, Carlos Eduardo Costa-Campos
Publikováno v:
Phyllomedusa: Journal of Herpetology, Vol 21, Iss 2 (2022)
Externí odkaz:
https://doaj.org/article/4923b7114187440db70fa4a3bc01e415
Akademický článek
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Publikováno v:
Case Reports in Ophthalmology, Vol 12, Iss 3, Pp 809-815 (2021)
Iris retraction syndrome (IRS) is an uncommon condition caused by retinal detachment that is characterized by back bowing of the peripheral iris, leading to a deep anterior chamber. It is commonly associated with ocular hypotony, ciliochoroidal detac
Externí odkaz:
https://doaj.org/article/ff0a22a9b3174d6d83df97ee0fb5677d
Publikováno v:
Dermatology Practical & Conceptual, Vol 12, Iss 4 (2022)
Externí odkaz:
https://doaj.org/article/8140cc934d9e4a91a2841653862440e5
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 16, Pp 295-299 (2021)
Purpose: We report a case with iris heterochromia misdiagnosed as Fuchs' uveitis which finally turned out to be a unilateral zoster uveitis in an HIV-positive patient. Case Report: A 45-year old patient was seen for a recurrent right anterior uveitis
Externí odkaz:
https://doaj.org/article/b36a916b821745e08e2b9dd76af80f69