TY - CHAP M1 - Book, Section TI - Laband Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Inherited polymalformative syndrome characterized by craniofacial anomalies with gingival fibromatosis and dystrophic fingers and fingernails. The clinical characteristics are gingival fibromatosis that is present at birth or in the days following it, severe hypoplasia of the distal phalanges of the hands and feet, dysplasia of the nail, joint hypermobility, and hepatosplenomegaly. Other features include a nose and pinnae usually large and poorly developed. It is often associated with mental retardation. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/05 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164076147 ER -