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- W1511451816 abstract "Papillon-Lefevre syndrome is a disorder of keratinization transmitted probably in an autosomal recessive fashion. Two brothers aged 7 and 4 1/2 years, of this syndrome is reported. Both had palmo-plantar keratoderma, early loss of teeth along with involvement of knees and elbows. There was no history of consanguinity between parents." @default.
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- W1511451816 date "2007-07-28" @default.
- W1511451816 modified "2023-09-23" @default.
- W1511451816 title "Papillon-Lefevre syndrome in two brothers." @default.
- W1511451816 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17656920" @default.
- W1511451816 hasPublicationYear "2007" @default.
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