TY - CHAP M1 - Book, Section TI - Schwartz-Jampel Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Marciniak, Bruno A1 - Dalens, Bernard J. PY - 2006 T2 - Syndromes: Rapid Recognition and Perioperative Implications AB - A very rare autosomal recessive condition manifested by a combination of muscle stiffness (hypertrophied muscle) and mild, largely nonprogressive muscle weakness (myotonia). Onset age is during the first year of life. Other clinical features include mostly ophthalmological anomalies and a pectus carinatum. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=58086331 ER -