Trochlear nerve agenesis in a patient with 18q22.2q23 deletion
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s10072-024-07554-0.pdf
Reference11 articles.
1. Yang HK, Gong HS, Hwang JM (2021) Congenital superior oblique palsy in a patient with Holt-Oram syndrome. Neurol Sci 42(1):373–375. https://doi.org/10.1007/s10072-020-04530-2
2. Yang HK, Kim JH, Hwang JM (2020) Combination of olfactory hypoplasia and superior oblique palsy: a previously unreported congenital cranial dysinnervation disorder. Neurol Sci 41(4):975–976. https://doi.org/10.1007/s10072-019-04114-9
3. Yang HK, Kim JH, Hwang JM (2012) Congenital superior oblique palsy and trochlear nerve absence: a clinical and radiological study. Ophthalmology 119(1):170–177. https://doi.org/10.1016/j.ophtha.2011.06.038
4. Kim JH, Hwang JM (2017) Imaging of cranial nerves III, IV, VI in congenital cranial dysinnervation disorders. Korean J Ophthalmol 31(3):183–193. https://doi.org/10.3341/kjo.2017.0024
5. Obara K, Inomata T (2023) 18q21.1q21.32 deletion in a patient with juvenile cerebral infarction. Cureus 15(7):e42534. https://doi.org/10.7759/cureus.42534
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