TY - CHAP M1 - Book, Section TI - Juvenile Hyaline Fibromatosis A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Rare congenital genetic disorder characterized by popular and nodular skin lesions, soft tissue masses, gingival hypertrophy, and joint contractures of the large articulations and bone involvement of variable complexity. The skin lesions are slow-growing soft masses, pearly white or skin-colored dermal papules or subcutaneous nodules mostly located on the face, scalp, and back. It is often confused for neurofibromatosis. It occurs from early childhood to adulthood. The disease has a relentlessly progressive course, with most patients surviving only up to the fourth decade. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/10 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164074439 ER -