RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164076147 T1 Laband Syndrome 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=1164076147 RD 2024/10/07 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.