TY - CHAP M1 - Book, Section TI - Riley-Smith Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A rare malformation syndrome characterized by Macrocephaly, Autosomal dominant, Thyroid disease, Cancer, Hamartomata, Skin abnormalities (MATCHS) and due to mutations of the PTEN tumor suppressor gene (an acronym that stands for Phosphatase and TENsin homolog deleted on chromosome TEN). Multiple hemangiomata and lipomas. Subcutaneous hemangioma may be present at birth or appear later in childhood. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164083727 ER -