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Papillon Lefevre syndrome.
Article in English | IMSEAR | ID: sea-94723
ABSTRACT
Papillon Lefèvre syndrome is a rare disease characterized by skin lesions caused by palmar-plantar hyperkeratosis, and severe periodontal destruction involving both the primary and permanent dentitions. It is transmitted as an autosomal recessive condition and consanguinity of parents is evident in about one-third of cases. Pyogenic liver abscess is an increasingly recognized complication. We report a new case of this association and review the current literature.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Papillon-Lefevre Disease / Periodontal Diseases / Chromosomes, Human, Pair 11 / Ceftriaxone / Humans / Male / Gentamicins / Adolescent / Keratoderma, Palmoplantar / Cathepsin C Language: English Year: 2006 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Papillon-Lefevre Disease / Periodontal Diseases / Chromosomes, Human, Pair 11 / Ceftriaxone / Humans / Male / Gentamicins / Adolescent / Keratoderma, Palmoplantar / Cathepsin C Language: English Year: 2006 Type: Article