Iridogoniodysgenesis (IGD) and Skeletal Anomalies
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_793-1
Reference4 articles.
1. Chrystal PW, Walter MA (2019) Aniridia and Axenfeld-Rieger syndrome: clinical presentations, molecular genetics and current/emerging therapies. Exp Eye Res 189:107815. https://doi.org/10.1016/j.exer.2019.107815
2. García-Cruz D, Mendoza R, Villar V et al (1990) A distinct dysmorphic syndrome with congenital glaucoma and probable autosomal recessive inheritance. Ophthalmic Paediatr Genet 11:35–40. https://doi.org/10.3109/13816819009012947
3. Mataftsi A (2016) Incidence of and risk factors for postoperative glaucoma and its treatment in paediatric cataract surgery. Dev Ophthalmol 57:40–48. https://doi.org/10.1159/000442500
4. Rodríguez-Rojas LX, García-Cruz D, Mendoza-Topete R et al (2004) Familial iridogoniodysgenesis and skeletal anomalies: a probable new autosomal recessive disorder. Clin Genet 66:23–29. https://doi.org/10.1111/j.0009-9163.2004.00271.x
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