Literature DB >> 2943312

A syndrome of keratosis palmo-plantaris congenita, pes planus, onychogryphosis, periodontosis, arachnodactyly and a peculiar acro-osteolysis.

J M Puliyel, K S Sridharan Iyer.   

Abstract

A family with a symptom complex of pes planus, onychogryphosis, palmoplantar hyperkeratosis and periodontosis is reported. A detailed pedigree is given and the mode of inheritance is suggested.

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Year:  1986        PMID： 2943312     DOI： 10.1111/j.1365-2133.1986.tb05725.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


  2 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

2.  Haim-Munk syndrome.

Authors:  Priyanka Pahwa; Arundeep K Lamba; Farrukh Faraz; Shruti Tandon
Journal:  J Indian Soc Periodontol       Date:  2010-07
  2 in total

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