Haim-Munk syndrome is an extremely rare autosomal recessive disorder characterized
clinically by palmoplantar hyperkeratosis, aggressive periodontitis with severe alveolar
bone destruction, onychogryphosis, pes planus, arachnodactyly, and acro-osteolysis.
Consanguinity seems a notable prerequisite. The aim of this study was therefore to
report one case of this syndrome and to focus on the periodontal manifestations, in
order to attract the attention of dental clinicians to this rare anomaly. (Eur J Dent
2010;4:338-340)
Keywords
Periodontitis - Haim-Munk syndrome - Palmoplantar keratoderma