TY - CHAP M1 - Book, Section TI - Sensenbrenner Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Ciliopathy. Autosomal recessive disorder characterized by dolichocephaly, sagittal suture synostosis, sparse and slow-growing fine hair, hypertelorism, nystagmus, taurodontia, dental fusion, anteverted nares, brachydactyly, clinodactyly, narrow thorax leading to respiratory problems, and mild mental retardation. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/11/08 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164084913 ER -