Zobrazeno 1 - 3
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pro vyhledávání: '"A Fathima Fahima"'
Autor:
R Padmapriya, Fathima Fahima Akbar
Publikováno v:
TNOA Journal of Ophthalmic Science and Research, Vol 62, Iss 3, Pp 358-360 (2024)
An 11-year-old boy presented with complaints of defective night vision. Visual acuity was 6/6 in both eyes. The fundus showed a golden-to-grey discoloration in light and on dark adaptation, the fundus reverted to its normal appearance demonstrating t
Externí odkaz:
https://doaj.org/article/e5726c4e008444d089a0b8c534a4f353
Autor:
M Hemanandini, A Fathima Fahima
Publikováno v:
TNOA Journal of Ophthalmic Science and Research, Vol 62, Iss 2, Pp 258-259 (2024)
Isolated sulphite oxidase deficiency is an autosomal recessive hereditary disorder. A 5-month-old male child with neonatal seizures and global developmental delay was referred by a paediatrician for ophthalmological evaluation. On examination, the ch
Externí odkaz:
https://doaj.org/article/2925ada880ac4b1585b3b34dff9bbb0b
Publikováno v:
Genomics & Genetics Weekly; 7/26/2024, p1269-1269, 1p