Congenital marked hypertrichosis and Laband syndrome in a child: overlap between the gingival fibromatosis-hypertrichosis and Laband syndromes
Lacombe, D.; Bioulac-Sage, P.; Sibout, M.; Daussac, E.; Lesure, F.; Manchart, J.P.; Battin, J.
Genetic Counseling 5(3): 251-256
1994
ISSN/ISBN: 1015-8146 PMID: 7811425 Document Number: 425222
Gingival fibromatosis may be reported as an isolated finding or associated with a number of distinct and frequently inherited group of disorders. The characteristics of the Laband syndrome include gingival hyperplasia, dysplasia of the terminal phalanges and nails of extremities, hepatosplenomegaly and facial dysmorphism. Another well-known syndrome with gingival fibromatosis associates generalized hypertrichosis and inconstant mental retardation and epilepsy. We report a case with features of Laband syndrome and congenital marked hypertrichosis, suggesting overlap between these two genetic disorders.