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| turner_syndrome [2025/07/16 04:28] – [Resources] Scott Larson | turner_syndrome [2025/10/01 15:18] (current) – Scott Larson |
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| * Anterior lenticonus | * Anterior lenticonus |
| * Retinal detachment | * Retinal detachment |
| * Mosaic Turner Findings | * Mosaic Turner reported ocular problems |
| * Anterior segment dysgenesis | * Anterior segment dysgenesis |
| * microphthalmia | * microphthalmia |
| * {{::turner_syndrome.pdf |Turner Syndrome: Ocular Manifestations and Considerations for Corneal Refractive Surgery. Moshifar Majid et al. J Clin Med. 2022;11:6853}} | * {{::turner_syndrome.pdf |Turner Syndrome: Ocular Manifestations and Considerations for Corneal Refractive Surgery. Moshifar Majid et al. J Clin Med. 2022;11:6853}} |
| * [[https://pubmed.ncbi.nlm.nih.gov/9349149/ |Anterior Segment Dysgenesis in Mosaic Turner Syndrome. Lloyd IC, Haigh PM, Clayton-Smith J, et al. The British Journal of Ophthalmology. 1997;81(8):639-43]] | * [[https://pubmed.ncbi.nlm.nih.gov/9349149/ |Anterior Segment Dysgenesis in Mosaic Turner Syndrome. Lloyd IC, Haigh PM, Clayton-Smith J, et al. The British Journal of Ophthalmology. 1997;81(8):639-43]] |
| * [[https://pubmed.ncbi.nlm.nih.gov/9737776/| Microphthalmia With Linear Skin Defects Syndrome in a Mosaic Female Infant With Monosomy for the Xp22 Region: Molecular Analysis of the Xp22 Breakpoint and the X-Inactivation Pattern. Ogata T, Wakui K, Muroya K, et al. Human Genetics. 1998;103(1):51-6] | * [[https://pubmed.ncbi.nlm.nih.gov/9737776/| Microphthalmia With Linear Skin Defects Syndrome in a Mosaic Female Infant With Monosomy for the Xp22 Region: Molecular Analysis of the Xp22 Breakpoint and the X-Inactivation Pattern. Ogata T, Wakui K, Muroya K, et al. Human Genetics. 1998;103(1):51-6]] |
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| {{tag>syndrome}} | {{tag>syndrome}} |