Report of 2 cases of Papillon Syndrome
نویسندگان
چکیده
منابع مشابه
Papillon-Lefevre syndrome: A report of two cases in a family
Palmoplantar keratodermas are a heterogenous group of diseases, one of them is Papillon-Lefevre Syndrome (PLS). This rare disease is inherited as autosomal recessive and characterized by focal hyperkeratotic plaques on elbows and knees, severe periodontal disease resulting in premature loss of teeth. We report two brothers with PLS who did not have a history of this disease in their famil...
متن کاملPapillon-Lefevre syndrome: A report of two cases
Papillon-Lefevre syndrome is a rare (1-4 cases per million) autosomal recessive disorder showing predominantly oral and dermatological manifestations in the form of aggressive periodontitis affecting both primary and permanent dentition and palmoplantar hyperkeratosis. Genetic studies have shown that mutations in the major gene locus of chromosome 11q14 with loss of function of cathepsin C gene...
متن کاملPapillon-Lefèvre Syndrome: a case report
Introduction: Papillon-Lefèvre syndrome(PLS) characterized by palmoplantar hyperkeratosis is a rare autosomal recessive genetic disorder with rapidly progressive periodontitis and premature loss of both deciduous and permanent teeth. In this study, we report the clinical and radiographic features of Papillon-Lefèvre syndrome in an 11- year-old girl and we also discuss the history ...
متن کاملPapillon-Lefèvre Syndrome Case Report
1 Assistant professor, Oro-maxillofacial developmental diseases research center, Department of oral medicine, Guilan University of Medical Sciences, Dental school, Rasht, Iran 2 Associate professor, Dental Research Center, Mashhad University of Medical Sciences, Dental School, Mashhad, Iran 3 Assistant professor, Department of Oral and Maxillofacial Radiology, Mashhad University of Medical Scie...
متن کاملNetherton syndrome: report of two cases
Netherton syndrome is a rare autosomal recessive condition with variable expression. It comprises an ichthyosiform dermatitis and erythroderma of variable intensity associated with hair abnormalities and features of atopy. The pathognomic (required for diagnosis) feature is trichorrhexis invaginata identified by microscopic examination of hair shaft. Ichthyosis linearis circumflexa is ano...
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ژورنال
عنوان ژورنال: Journal of North Khorasan University of Medical Sciences
سال: 2011
ISSN: 2008-8698,2008-8701
DOI: 10.29252/jnkums.3.1.12