RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164086685 T1 Tricho-Rhino-Phalangeal Dysplasia Type III T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164086685 RD 2024/10/06 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.