Oral Care in Kindler Syndrome: 7-Year Follow-up of 2 Brothers - Archive ouverte HAL
Article Dans Une Revue Journal of Clinical Pediatric Dentistry Année : 2021

Oral Care in Kindler Syndrome: 7-Year Follow-up of 2 Brothers

Résumé

Background: Kindler poikiloderma is an inherited autosomal genodermatosis characterized by blistering of the epidermis and mucosae. Its prevalence is unknown. Case report: We monitored two brothers suffering from this pathology. Oral manifestations mainly take the form of periodontal lesions. In our patients we noted gingivitis progressing to periodontitis as follow-up care was not effective. We also diagnosed enamel hypoplasia, described more rarely in this pathology. Conclusion: Periodontitis in Kindler Syndrome responds to maintenance therapy, but the absence of surveillance is penalized by a deterioration in periodontal condition and complication of management. All restorative, endodontic, surgical, periodontal and orthodontic treatments should be performed with appropriate precautions.
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hal-03825988 , version 1 (28-10-2022)

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Isabelle Blanchet, Corinne Tardieu, Estelle Casazza. Oral Care in Kindler Syndrome: 7-Year Follow-up of 2 Brothers. Journal of Clinical Pediatric Dentistry, 2021, 45 (1), pp.41 - 47. ⟨10.17796/1053-4625-45.1.8⟩. ⟨hal-03825988⟩
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