Literature DB >> 7544664

Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneity.

D P Kelsell1, H P Stevens, R Ratnavel, S P Bryant, D T Bishop, I M Leigh, N K Spurr.   

Abstract

The palmoplantar keratodermas (PPK) are a group of skin diseases characterized by thickening of the skin of the palms and soles due to abnormal keratinization. We have performed linkage analysis on families affected with three distinct forms of non-epidermolytic PPK (NEPPK): focal, diffuse and punctate. Genetic heterogeneity was demonstrated, with focal NEPPK linked to the region on chromosome 17 harbouring the type I keratin cluster, diffuse NEPPK linked to the region on chromosome 12 containing the type II keratin cluster, and in the punctate NEPPK pedigrees, linkage was excluded to both of these keratin clusters. This study provides evidence for genetic differences between these forms of NEPPK and also between NEPPK and epidermolytic PPK (EPPK) in which mutations in keratin 9 have been demonstrated.

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Year:  1995        PMID: 7544664     DOI: 10.1093/hmg/4.6.1021

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  5 in total

1.  High-resolution transcript map of the region spanning D12S1629 and D12S312 at chromosome 12q13: triple A syndrome-linked region.

Authors:  H Lee; E Choi; Y Seomun; K Montgomery; A Huebner; E Lee; S Lau; C K Joo; R Kucherlapati; S J Yoon
Journal:  Genome Res       Date:  2000-10       Impact factor: 9.043

2.  Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24.

Authors:  A Martinez-Mir; A Zlotogorski; D Londono; D Gordon; A Grunn; E Uribe; L Horev; I M Ruiz; N O Davalos; O Alayan; J Liu; T C Gilliam; J C Salas-Alanis; A M Christiano
Journal:  J Med Genet       Date:  2003-12       Impact factor: 6.318

Review 3.  The molecular basis for inherited bullous diseases.

Authors:  B P Korge; T Krieg
Journal:  J Mol Med (Berl)       Date:  1996-02       Impact factor: 4.599

4.  Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratoderma.

Authors:  Diana C Blaydon; Lisbet K Lind; Vincent Plagnol; Kenneth J Linton; Francis J D Smith; Neil J Wilson; W H Irwin McLean; Colin S Munro; Andrew P South; Irene M Leigh; Edel A O'Toole; Anita Lundström; David P Kelsell
Journal:  Am J Hum Genet       Date:  2013-07-03       Impact factor: 11.025

5.  The first Danish family reported with an AQP5 mutation presenting diffuse non-epidermolytic palmoplantar keratoderma of Bothnian type, hyperhidrosis and frequent Corynebacterium infections: a case report.

Authors:  Anne Bruun Krøigård; Liv Eline Hetland; Ole Clemmensen; Diana C Blaydon; Jens Michael Hertz; Anette Bygum
Journal:  BMC Dermatol       Date:  2016-06-03
  5 in total

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