syndrome

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Related to Papillon-Lefevre Syndrome: Papillon-Lefèvre syndrome
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Localization of a gene for Papillon-Lefevre syndrome to chromosome 11q14-q21 by homozygosity mapping.
Behavior of neutrophilic granulocytes in a case of Papillon-Lefevre syndrome.
Dermatologic and oral findings in a cohort of 47 patients with Papillon-Lefevre syndrome.
Occurrence of Actinobacillus actinomycetemcomitans and anti-leukotoxin antibodies in some members of an extended family affected by Papillon-Lefevre syndrome.
Evidence for a founder mutation in the cathepsin C gene in three families with Papillon-Lefevre syndrome.
Lowered activity of cathepsin C might not cause full-blown Papillon-Lefevre syndrome, but it might cause periodontitis-with less-efficient cleaning up of the plaque bacteria," he says.
Clinical, bacteriological, and immunological examinations and the treatment process of two Papillon-Lefevre syndrome patients.
Long-term preservation of permanent teeth in a patient with Papillon-Lefevre syndrome treated with etretinate.
The phenotypic expression of Papillon-Lefevre syndrome is heterogeneous as regards to the severity of the dermatological as well as the periodontal symptoms.
A genetic study of cathepsin C gene in two families with Papillon-Lefevre syndrome.
Suggested mode of periodontal therapy for patients with Papillon-Lefevre syndrome.
Clinical, genetic, and biochemical findings in two siblings with Papillon-Lefevre syndrome.
Microbiological and serological investigation of oral lesions in Papillon-Lefevre syndrome.