Literature DB >> 162525

A genetic analysis of the Papillon-Lefèvre syndrome in a Jewish family from Cochin.

S Hacham-Zadeh, T Schaap, M M Cohen.   

Abstract

The Papillon-Lefèvre syndrome (PLS) is segregating in a large kindred of a Jewish isolate originating from Cochin, India. The frequency of the gene responsible for PLS among the Cochin Jews, 0.1, was estimated from the number of unrelated carriers in the isolate who married into the kindred. The obvious discrepancy between this apparently high gene frequency and the total absence of PLS in other kindreds of the isolate suggests that the syndrome may not behave as a simple autosomal recessive trait.

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Year:  1978        PMID: 162525     DOI: 10.1002/ajmg.1320020206

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  4 in total

1.  Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C.

Authors:  T C Hart; P S Hart; M D Michalec; Y Zhang; E Firatli; T E Van Dyke; A Stabholz; A Zlotogorski; L Shapira; W A Soskolne; A Zlorogorski
Journal:  J Med Genet       Date:  2000-02       Impact factor: 6.318

Review 2.  The Papillon-Lefèvre syndrome: keratosis palmoplantaris with periodontopathy. Report of a case and review of the cases in the literature.

Authors:  E Haneke
Journal:  Hum Genet       Date:  1979-09-02       Impact factor: 4.132

3.  Immunological study of patients with the Papillon--Lefevre syndrome.

Authors:  Y Levo; S Wollner; S Hacham-Zadeh
Journal:  Clin Exp Immunol       Date:  1980-05       Impact factor: 4.330

4.  Heterozygous Ile453Val codon mutation in exon 7, homozygous single nucleotide polymorphisms in intron 2 and 5 of cathepsin C are associated with Haim-Munk syndrome.

Authors:  Nalini Aswath; Bhuminathan Swamikannu; Sankar Narayanan Ramakrishnan; Rajendran Shanmugam; Jayakar Thomas; Arvind Ramanathan
Journal:  Eur J Dent       Date:  2014-01
  4 in total

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