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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Idiopathic familial gingival fibromatosis associated with mental retardation, epilepsy and hypertrichosis.

Gingival fibromatosis, a rare but often familial condition, is described in two siblings, associated with mental retardation, epilepsy and hypertrichosis. In one child a maxillary giant-cell tumour was found and excised. It is important to distinguish idiopathic gingival fibromatosis from phenytoin-induced gingival hypertrophy.[1]

References

  1. Idiopathic familial gingival fibromatosis associated with mental retardation, epilepsy and hypertrichosis. Anavi, Y., Lerman, P., Mintz, S., Kiviti, S. Developmental medicine and child neurology. (1989) [Pubmed]
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