TY - CHAP M1 - Book, Section TI - Krause-Reese Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is an inherited syndrome characterized by multiple ocular malformations in association with microcephaly. It is more commonly found in premature infants and in single infants of multiple births. It is characterized by the presence of retinal and cerebral dysplasia, microphthalmos, retinal choroid and optic nerve malformations, retinal glial membranes, hyperplasia or aplasia of the brain and cerebellum, and microcephaly. Other features include mental retardation, hydrocephalus, blindness, enophthalmos, microphthalmos, strabismus, retinal atrophy, gliosis, retinal and vitreous hemorrhages, synechiae, glaucoma, and cataract. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164075913 ER -