TY - CHAP M1 - Book, Section TI - Mauriac Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a very rare metabolic disorder characterized by early onset of diabetes mellitus in the infancy period, cushingoid features (moon face-like appearance), multiple epiphyseal dysplasia, multiple fractures, microcephaly, short stature, hypertonia, barrel-shaped chest, hepatomegaly, tooth discoloration, gray-blue sclerae, high-arched palate, and skin abnormalities. Epiphyseal dysplasia and growth retardation have onset within the first 2 years of life. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/11/02 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164077978 ER -