TY - CHAP M1 - Book, Section TI - Eronen Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a very rare disorder inherited as an autosomal recessive pattern and characterized by the absence or severe digital phalanges abnormalities of the fingers and toes, renal defects, and cerebral malformations, particularly ventricles dilatation, raised intracranial pressure, and prolonged seizures. Affected individuals present profound intellectual disabilities. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164069127 ER -