TY - CHAP M1 - Book, Section TI - Granddad Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A medical condition characterized by the mnemonic growth retardation, aged facial appearance, normal development, decreased subcutaneous fat, and inherited as an autosomal dominant inheritance. The clinical presentation is associated with characteristic facial appearance that includes triangular facies, prominent forehead, thin or absent scalp hair, deep-set eyes, midfacial hypoplasia, prominent nasal septum with hypoplasia of the alae nasi, prominent ears, and thin lips. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164071536 ER -