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Periodontal Manifestation in a Patient with Kindler Syndrome

Kindler syndrome is a rare subtype of inherited epidermolysis bullosa. A 42-year-old female patient was admitted to our clinic with a complaint of tooth mobility. Multiple hypo- and hyperpigmented macules dissipated all over her body, prominent poikilodermatous changes, xerosis of the skin, and atro...

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Dades bibliogràfiques
Publicat a:Case Rep Dent
Autors principals: Sari, Aysegul, Celik, Salih
Format: Artigo
Idioma:Inglês
Publicat: Hindawi 2021
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7963901/
https://ncbi.nlm.nih.gov/pubmed/33763263
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2021/6671229
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