TY - CHAP M1 - Book, Section TI - Osteopetrosis A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Heterogenous genetic disorder of bone metabolism characterized by deficient osteoclast function with defective bone resorption and increased bone mass. Depending on the mode of inheritance, its course can be either uniformly fatal with pancytopenia, recurrent pathologic fractures, blindness, and other neurologic symptoms, or it can exist in a much milder form with later manifestation and favorable prognosis. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164080823 ER -