Aniridia Guides and Aniridia-Syndrome (PAX6-Syndrome): Do’s and Dont’s in Clinical Care
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Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-19779-1_14
Reference27 articles.
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2. Bamiou DE, Free SL, Sisodiya SM, Chong WK, Musiek F, Williamson KA, van Heyningen V, Moore AT, Gadian D, Luxon LM (2007) Auditory interhemispheric transfer deficits, hearing difficulties, and brain magnetic resonance imaging abnormalities in children with congenital aniridia due to PAX6 mutations. Arch Pediatr Adolesc Med 161(5):463–469
3. Hingorani M, Hanson I, van Heyningen V (2012) Aniridia. Eur J Hum Genet 20(10):1011–1017
4. Peter NM, Leyland M, Mudhar HS, Lowndes J, Owen KR, Stewart H (2013) PAX6 mutation in association with ptosis, cataract, iris hypoplasia, corneal opacification and diabetes: a new variant of familial aniridia? Clin Exp Ophthalmol 41(9):835–841
5. Beby F, Dieterich K, Calvas P (2011) A [c.566-2A>G] heterozygous mutation in the PAX6 gene causes aniridia with mild visual impairment. Eye (Lond) 25(5):657–658
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1. Psychoneurological Disorders in Children with Congenital Aniridia and <i>PAX6</i>-Associated Syndromes;Current Pediatrics;2023-08-25
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