Secondary Childhood glaucoma – a rare association in Seckel syndrome
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A case of 12-year-old male with Seckel syndrome, presented with unilateral glaucoma leading to advanced disc damage hence, visual deterioration. Seckel syndrome being a rare inherited disorder characterized by growth delay and unique facial features, had been infrequently reported for ophthalmic anifestation especially glaucoma. Though glaucoma is a rare association in Seckel syndrome, screening at an early stage could help in preventing vision loss.
2019 ◽
Vol 9
(2)
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pp. 5508-5512
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2007 ◽
Vol 4
(3_suppl)
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pp. S9-S11
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2019 ◽
Vol 9
(2)
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pp. 3984-3987
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2021 ◽
Vol 11
(12)
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pp. 3082-3089
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2010 ◽
Vol 51
(2)
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pp. 139-141
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2020 ◽
Vol 21
(17)
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pp. 6243
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