Add to ORKGPapillon-Lefèvre syndrome (PLS) is an autosomal recessive condition with palmoplantar hyperkeratosis and aggressive periodontitis as cardinal features. The disorder is linked to mutations of the gene for cathepsin C, a lysosomal protease essential in activation of serine proteases in immune and inflammatory cells. The genetic background of the disorder has been identified, but its relation to phenotypic expression is obscure. The aims of the project were to explore phenotypic expression in young patients with PLS, and to investigate any correlation between clinical expression and identified genotype. Additionally, biochemical properties of gingival crevicular fluid (GCF) were investigated, and the result of an oral treatment protocol based...
Background : Loss-of-function point mutations in the cathepsin C gene are the underlying genetic eve...
AbstractPapillon–Lefevre syndrome (PLS) is a very rare, autosomal recessive syndrome characterized b...
Papillon-Lefevre syndrome (PLS) is an inherited human disease characterized by early-onset periodont...
Papillon-Lefévre syndrome (PLS) is a very rare autosomal recessive trait characterized by palmoplant...
Papillon-Lefëvre syndrome (PLS), classified as ectodermal dysplasia, is an autosomal recessive condi...
Background: Papillon-Lefèvre syndrome (PLS) is a rare autosomal recessive genodermatosis characteriz...
Papillon–Lefevre syndrome (PLS) is a extreme rare of autosomal recessive inheritance characterized b...
Introduction: Papillon-Lefèvre syndrome is a rare autosomal recessive disorder. This syndrome is cha...
OBJECTIVES: Numerous patients with Papillon-Lefevre syndrome (PLS) express a severe periodontal infl...
Papillon–Lefevre syndrome (PLS) is a rare autosomal recessive disorder, showing oral and dermatologi...
Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by palmoplantar hyp...
BACKGROUND Loss-of-function point mutations in the cathepsin C gene are the underlying genetic ev...
Papillion-Lefèvre Syndrome is a very rare disorder of autosomal recessive inheritance distinguished ...
The aim of this thesis was to elucidate factors possibly contributing to the rapidly progressing per...
Papillon-Lefèvre syndrome (PLS) (OMIM: 245000) is a rare disease characterized by severe periodontit...
Background : Loss-of-function point mutations in the cathepsin C gene are the underlying genetic eve...
AbstractPapillon–Lefevre syndrome (PLS) is a very rare, autosomal recessive syndrome characterized b...
Papillon-Lefevre syndrome (PLS) is an inherited human disease characterized by early-onset periodont...
Papillon-Lefévre syndrome (PLS) is a very rare autosomal recessive trait characterized by palmoplant...
Papillon-Lefëvre syndrome (PLS), classified as ectodermal dysplasia, is an autosomal recessive condi...
Background: Papillon-Lefèvre syndrome (PLS) is a rare autosomal recessive genodermatosis characteriz...
Papillon–Lefevre syndrome (PLS) is a extreme rare of autosomal recessive inheritance characterized b...
Introduction: Papillon-Lefèvre syndrome is a rare autosomal recessive disorder. This syndrome is cha...
OBJECTIVES: Numerous patients with Papillon-Lefevre syndrome (PLS) express a severe periodontal infl...
Papillon–Lefevre syndrome (PLS) is a rare autosomal recessive disorder, showing oral and dermatologi...
Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by palmoplantar hyp...
BACKGROUND Loss-of-function point mutations in the cathepsin C gene are the underlying genetic ev...
Papillion-Lefèvre Syndrome is a very rare disorder of autosomal recessive inheritance distinguished ...
The aim of this thesis was to elucidate factors possibly contributing to the rapidly progressing per...
Papillon-Lefèvre syndrome (PLS) (OMIM: 245000) is a rare disease characterized by severe periodontit...
Background : Loss-of-function point mutations in the cathepsin C gene are the underlying genetic eve...
AbstractPapillon–Lefevre syndrome (PLS) is a very rare, autosomal recessive syndrome characterized b...
Papillon-Lefevre syndrome (PLS) is an inherited human disease characterized by early-onset periodont...