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....

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Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Erciyas, Kamile, Inaloz, Serhat, Erciyas, A. Fuat
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Dental Investigations Society 2010
Konular:
Case Reports
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2897870/
https://ncbi.nlm.nih.gov/pubmed/20613925
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