Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Karthikeyan Arcot Sadagopan"'
Publikováno v:
Oman Journal of Ophthalmology, Vol 14, Iss 2, Pp 115-116 (2021)
Externí odkaz:
https://doaj.org/article/e69eb09332a24b70a71d26c3ed804788
Publikováno v:
Ophthalmic Genetics. 44:54-69
Oculocutaneous albinism (OCA) could be either non-syndromic or syndromic. There are significant challenges in clinically recognizing and differentiating Hermansky-Pudlak syndrome (HPS) from non-syndromic OCA.In a prospective consecutive case series,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::177c22a2f3a117b81705e5f442b7c0f1
https://doi.org/10.1080/13816810.2022.2135109
https://doi.org/10.1080/13816810.2022.2135109
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 24:172-175
Abnormalities in extraocular muscle insertions, such as bilateral bifid superior rectus insertion, have been reported in albinism; however, abnormalities of the inferior oblique insertion have not been described previously. We report abnormal inferio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::421c800f691545d23c9cb1ac6bff538f
https://doi.org/10.1016/j.jaapos.2020.01.011
https://doi.org/10.1016/j.jaapos.2020.01.011
Publikováno v:
Journal of binocular vision and ocular motility. 71(1)
Binocular triplopia is a rare symptom and usually has a corneal or lenticular origin. Uniocular diplopia arising from ectopia lentis is quite common in Marfan syndrome. A visual phenomenon related to binocular triplopia due to strabismus was first re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1af94dacda1a7430fee2d8aff77854d2
https://pubmed.ncbi.nlm.nih.gov/33566747
https://pubmed.ncbi.nlm.nih.gov/33566747
Publikováno v:
Oman Journal of Ophthalmology
Oman Journal of Ophthalmology, Vol 14, Iss 2, Pp 115-116 (2021)
Oman Journal of Ophthalmology, Vol 14, Iss 2, Pp 115-116 (2021)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3198d7e70a89bbf510e2371f15363b96
http://europepmc.org/articles/PMC8300293
http://europepmc.org/articles/PMC8300293
A new surgical 'noose' technique for excision of pediatric ocular adnexal and anterior orbital cysts
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 19:372-375
We describe a "noose technique" that facilitates complete surgical excision of all forms of pediatric adnexal and anterior orbital extraocular cysts, including conjunctival retention cysts, parasitic cysts involving the conjunctiva, Tenon's capsule,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0b64b6f70aa3880be71189bf7aba700
https://doi.org/10.1016/j.jaapos.2015.02.018
https://doi.org/10.1016/j.jaapos.2015.02.018
Autor:
Jenina E. Capasso, Rosanne B Keep, Karthikeyan Arcot Sadagopan, Wadakarn Wuthisiri, Alex V. Levin, Grace T. Liu
Publikováno v:
American Journal of Medical Genetics Part A. 167:524-528
Axenfeld–Rieger spectrum (ARS) includes the anterior segment abnormalities posterior embryotoxon, irido-corneal adhesions, corectopia, and other abnormalities of pupil size and shape. Glaucoma occurs in approximately 50% of affected children. It is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed6f76d1affff77a1a8c348d64220b40
https://doi.org/10.1002/ajmg.a.36890
https://doi.org/10.1002/ajmg.a.36890
Autor:
Karthikeyan Arcot Sadagopan
Publikováno v:
Current opinion in ophthalmology. 28(5)
The purpose of this review is to outline those systemic disorders that are associated with pediatric retinal dystrophy, summarize important retinal, and nonretinal clues that aid in syndromic diagnosis, provide an approach for ophthalmic and systemat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a730138c66e78e8f1ed1f8b438a90f8
https://pubmed.ncbi.nlm.nih.gov/28650875
https://pubmed.ncbi.nlm.nih.gov/28650875
Publikováno v:
Current Opinion in Ophthalmology. 24:438-447
To provide clinically relevant information regarding the evaluation and current treatment options for oculomotor nerve palsies. We survey recent literature and provide some insights into these studies.Recent case reports highlight emerging new causes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdd86b9d38ae92df9d20472a6aeb9d30
https://doi.org/10.1097/icu.0b013e3283645a9b
https://doi.org/10.1097/icu.0b013e3283645a9b
Autor:
Kannan Parthiban, Arndt Rolfs, Hui Huang, Renugadevi Kathirvel, Rosanne B Keep, Periasamy Sundaresan, Perumalsamy Vijayalakshmi, Karthikeyan Arcot Sadagopan
Publikováno v:
Ophthalmic genetics. 38(2)
Hermansky-Pudlak syndrome (HPS; MIM #203300) is a rare autosomal recessive disorder characterized by oculocutaneous albinism (OCA) and a bleeding diathesis. Other clinical features may include lyso...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0749d9fc46f69e0dd4c57d01015e42cf
https://pubmed.ncbi.nlm.nih.gov/27484007
https://pubmed.ncbi.nlm.nih.gov/27484007