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--- turner_syndrome [2025/04/14 03:25] – [Main Features] Scott Larson
+++ turner_syndrome [2025/10/01 15:18] (current) – Scott Larson
@@ Line 4: / Line 4: @@
   * Short stature
   * Webbed neck
-  * "shield chest" with wide-spaced nipples
+  * "Shield chest" with wide-spaced nipples
   * cubitus valgus
   * hearing loss
@@ Line 25: / Line 25: @@
     * Anterior lenticonus
     * Retinal detachment
-  * Mosaic Turner Findings
+  * Mosaic Turner reported ocular problems
     * Anterior segment dysgenesis
     * microphthalmia
@@ Line 37: / Line 37: @@
 ====Resources====
   * {{::turner_syndrome.pdf |Turner Syndrome: Ocular Manifestations and Considerations for Corneal Refractive Surgery. Moshifar Majid et al. J Clin Med. 2022;11:6853}}
-  * 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. doi:10.1136/bjo.81.8.639. https://pubmed.ncbi.nlm.nih.gov/9349149/
+  *  [[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]]
-  * 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. doi:10.1007/s004390050782. https://pubmed.ncbi.nlm.nih.gov/9737776/
+  * [[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]]
 {{tag>syndrome}}

syndrome