Periodontal manifestations in a patient with haim-munk syndrome
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Updated: Jun 11, 2026

Robust Ligature-Induced Model of Murine Periodontitis for the Evaluation of Oral Neutrophils
Published on: January 21, 2020
Kamile Erciyas1, Serhat Inaloz, A Fuat Erciyas
1Assistant Professor, Gaziantep University, Faculty of Dentistry, Department of Periodontology, Gaziantep, Turkey.
Abstract:
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.
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