TY - CHAP M1 - Book, Section TI - Knobloch Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - An inherited disorder characterized by encephalocele, vitreoretinal degeneration with retinal detachment, high myopia, and normal intelligence. It is also characterized by cataracts, and the association with skull defects such as occipital encephalocele and occipital aplasia. Meningocele have also been reported as part of this medical disorder. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164075558 ER -