Literature DB >> 17194569

Striate palmoplantar keratoderma resulting from a frameshift mutation in the desmoglein 1 gene.

Alison G Barber1, Muhammad Wajid, Morgana Columbo, Jillian Lubetkin, Angela M Christiano.   

Abstract

BACKGROUND: Striate keratodermas (PPKS) are a group of rare autosomal dominant palmoplantar keratodermas, characterized by a thickening of the skin on the palms and soles. PPKS is characterized by hyperkeratosis extending along the length of each finger and on the palm of the hand, as well as by patches of hyperkeratosis on the soles.
OBJECTIVE: We report a four-generation Pakistani kindred in which 11 members were affected with PPKS.
METHODS: Based on previous reports of DSG1 mutations in PPKS, we performed direct DNA sequencing analysis.
RESULTS: Clinically, these patients presented with hyperkeratotic palms and with linear hyperkeratosis on the fingers. Additionally, focal hyperkeratosis was seen on the sole of the toes as well as the ball and heel of the foot. DNA sequencing analysis revealed a heterozygous G-to-T transversion in the 3' splice acceptor site of intron 11 of the DSG1 gene designated 1688 -1 G>T. We predict that this mutation will lead to the skipping of exon 12 which is out of frame (134nt), subsequent degradation of the mutant mRNA by non-sense mediated RNA decay, and haploinsufficiency for DSG1.
CONCLUSION: We report a novel splice site mutation in the DSG1 gene in PPKS, which further underscores the significance of the desmoglein gene family in diseases of epidermal integrity.

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Year:  2006        PMID: 17194569      PMCID: PMC2914539          DOI: 10.1016/j.jdermsci.2006.11.013

Source DB:  PubMed          Journal:  J Dermatol Sci        ISSN: 0923-1811            Impact factor:   4.563


  19 in total

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3.  Frameshift mutation in the V2 domain of human keratin 1 results in striate palmoplantar keratoderma.

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5.  Mutations in the desmoglein 1 gene in five Pakistani families with striate palmoplantar keratoderma.

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