Visual outcomes in children with syndromic craniosynostosis: a review of 165 cases
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
http://www.nature.com/articles/s41433-021-01458-5.pdf
Reference21 articles.
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2. Kressa W, Collmann H. Saethre-chotzen syndrome: clinical and molecular genetic aspects. In: Muenke M, Kress W, Collmann H, Solomon BD, editors. Monographs in human genetics. Basel: Karger; 2011. vol. 19, pp. 98–106. https://doi.org/10.1159/isbn.978-3-8055-9595-7
3. Muenke M, Kress W, Collman H, Solomon BD. Craniosynostoses: molecular genetics, principles of diagnosis, and treatment. Basel, Switzerland: S. Karger; 2011
4. Khan SH, Nischal KK, F Dean F, Hayward RD, Walker J. Visual outcomes and amblyogenic risk factors in craniosynostotic syndromes: a review of 141 cases. Br J Ophthalmol. 2003;87:999–1003.
5. Liasis A, Thompson DA, Hayward R, Nischal KK. Sustained raised intracranial pressure implicated only by pattern reversal visual evoked potentials after cranial vault expansion surgery. Pediatr Neurosurg. 2003;39:75–80.
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