GRIPE
发表于 2025-3-25 07:11:55
Congenital Stationary Night Blindness,3]. Other associated abnormalities are color vision defect, nystagmus, photophobia, strabismus, refractive error, and fundus abnormality . Clinical presentation may appear differently depending on the causative gene.
Terrace
发表于 2025-3-25 08:05:59
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巨大没有
发表于 2025-3-25 12:38:55
https://doi.org/10.1007/978-981-16-7337-5Inherited retinal disease; retinitis pigmentosa; retinal dystrophy; genetic diagnosis; molecular genetic
Cholesterol
发表于 2025-3-25 16:23:36
Hyeong-Gon YuUpdates on clinical features and molecular diagnosis.Cases contributed by global leaders in the field.Clinical photographs obtained with newer imaging techniques.Many images of rare but clinically imp
jeopardize
发表于 2025-3-25 23:32:03
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synovium
发表于 2025-3-26 03:24:57
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外形
发表于 2025-3-26 07:44:08
Leber Congenital Amaurosis/Early-Onset Severe Retinal Dystrophy,al diseases with widely overlapping features. Herein we present in a comprehensive and concise manner the clinical features, molecular genetics, treatment principles, novel treatment methods, and retinal imaging findings of LCA/EOSRD, emphasizing in some of the most common genotypes: ., ., ., ., ., ., ., and
笨拙的我
发表于 2025-3-26 08:41:17
Cone Dystrophy/Cone-Rod Dystrophy,earance. The loss of cones leads to predominant symptoms such as decreased visual acuity, color vision defects and day blindness. Cone dystrophies are genetically heterogeneous and can be inherited by autosomal recessive, autosomal dominant or X-linked recessive patterns.
激怒某人
发表于 2025-3-26 12:37:16
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pester
发表于 2025-3-26 17:52:08
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