Accepted at 4:14 p.m. Oct, 31, 2023
Author: verdictologist
Related Note: 1603050798832
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One form of recessive optic atrophy is {{c1::Wolfram syndrome}} which is due to biallelic mutations of {{c2::WFS1}}. It is associated with non-ocular findings of {{c3::hearing loss}} and {{c3::diabetes}}.
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#Blue::#Resources::BCSC::06-Pediatrics-and-Strabismus::23-Optic-Nerve-Head-Abnormalities #Blue::#Topics::Pediatric_Childhood::Ocular-manifestations-of-systemic-disease-Pediatrics #Blue::#Topics::Pediatric_Childhood::Optic-disc-Abnormalities-Pediatrics #Blue::#Resources::BCSC::BCSC_high-yield #Blue::#Resources::BCSC::06-Pediatrics-and-Strabismus::27-Ocular-Manifestations-of-Systemic-Disease