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|15:45||K. Arcot Sadagopan ChinaA new clinical sign “The freckle sign”, a possible clinical marker for the diagnosis of Hermansky Pudlak syndrome in Indian patients with oculocutaneous albinism|
|15:51||B. Käsmann-Kellner GermanyAniridia or PAX6 syndrome: clinical findings, problematic courses especially concerning aniridic glaucoma and suggestions for refining the care (“aniridia guide”)|
|15:57||L. Wulandari IndonesiaRho Kinase inhibitor Y-27632 decrease expression of caspase-3 retinal ganglion cells in rat model glaucoma induced with sodium hyaluronate|
|16:03||K. Arcot Sadagopan ChinaThe clinical phenotypic spectrum of paediatric Cohen syndrome (CS) in Indian Patients as compared to Finnish and other non-Finnish ethnic cohorts|
|16:09||S. Zhang ChinaA novel FGFR2 genetic mutation associated with Crouzon syndrome in a Chinese family|
|16:15||J. Matalia IndiaA novel idea of identification of regulatory pathways in paediatric cataract: a pilot study|
|16:21||G. Bacci ItalyEarly onset X-linked retinoschisis in monozygotic twins: a multimodal diagnostic approach|
|16:27||A. Pakhomova UkraineAnterior segment ultrasound changes in patients with Ehlers-Danlos syndrome|
|16:33||A. Medsinge USAVertical nystagmus in two siblings with autosomal recessive congenital stationary night blindness: a rare presentation with novel mutations|
|16:39||M. Ortube USAThree atypical phenotype-genotype associations in paediatric cases|
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