TY - CHAP M1 - Book, Section TI - Tricho-Rhino-Phalangeal Dysplasia Type III A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - An extremely rare inherited multisystem disorder characterized by fine, thin light-colored hair, unusual facial features, abnormalities of the fingers and/or toes, and multiple abnormalities of epiphyses leading to skeletal dysplasia. The skeletal dysplasia is mostly observed in the hands and feet. There are no exostoses. Normal intelligence. Severe end of TRPS spectrum. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/06 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164086685 ER -