TY - CHAP M1 - Book, Section TI - Haim-Munk Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Haim-Munk Syndrome is an extremely rare autosomal recessive disorder of keratinization characterized clinically by palmoplantar hyperkeratosis, pyogenic skin lesions, severe early onset periodontitis, onychogryphosis, pes planus, arachnodactyly, and acroosteolysis. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/11/04 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164071897 ER -