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Periodontal Manifestations in a Patient with Haim-Munk Syndrome
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....
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Dental Investigations Society
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2897870/ https://www.ncbi.nlm.nih.gov/pubmed/20613925 |