TY - CHAP M1 - Book, Section TI - Donohue Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is an extremely rare inherited condition caused by resistance to insulin with growth deficiency and characterized by dysmorphic facies (“elfin-like”), severe growth retardation, hirsutism, and multiple endocrine disorders. Other features include low birth weight, skin abnormalities (acanthosis nigricans and pachyderma), and significant enlargement of the breast and clitoris in females and the penis in males. Hypertrophic cardiomyopathy has also been observed in these patients. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164068230 ER -