The molecular genetic analysis of the expanding pachyonychia congenita case collection

• Published in: British journal of dermatology (1951) Vol. 171; no. 2; pp. 343 - 355
• Main Authors: Wilson, N.J., O'Toole, E.A., Milstone, L.M., Hansen, C.D., Shepherd, A.A., Al-Asadi, E., Schwartz, M.E., McLean, W.H.I., Sprecher, E., Smith, F.J.D.
• Format: Journal Article
• Language: English
• Published: Oxford Blackwell Publishing Ltd 01.08.2014; Wiley-Blackwell; BlackWell Publishing Ltd
• Subjects: Biological and medical sciences; Dermatology; Humans; Keratin-16 - genetics; Keratin-17 - genetics; Keratin-6 - genetics; Keratins - genetics; Medical sciences; Mutation - genetics; Original; Pachyonychia Congenita - genetics; Pedigree; Skin disease; Expanding; Dermatology; Nail disease; Genetics; Pachyonychia; Molecular biology; Congenital disease
• ISSN: 0007-0963; 1365-2133
• DOI: 10.1111/bjd.12958

Summary Background Pachyonychia congenita (PC) is a rare autosomal dominant keratinizing disorder characterized by severe, painful, palmoplantar keratoderma and nail dystrophy, often accompanied by oral leucokeratosis, cysts and follicular keratosis. It is caused by mutations in one of five keratin genes: KRT6A, KRT6B, KRT6C, KRT16 or KRT17. Objectives To identify mutations in 84 new families with a clinical diagnosis of PC, recruited by the International Pachyonychia Congenita Research Registry during the last few years. Methods Genomic DNA isolated from saliva or peripheral blood leucocytes was amplified using primers specific for the PC‐associated keratin genes and polymerase chain reaction products were directly sequenced. Results Mutations were identified in 84 families in the PC‐associated keratin genes, comprising 46 distinct keratin mutations. Fourteen were previously unreported mutations, bringing the total number of different keratin mutations associated with PC to 105. Conclusions By identifying mutations in KRT6A, KRT6B, KRT6C, KRT16 or KRT17, this study has confirmed, at the molecular level, the clinical diagnosis of PC in these families. What's already known about this topic? Pachyonychia congenita (PC) is caused by autosomal dominant mutations in KRT6A, KRT6B, KRT6C, KRT16 or KRT17. Plantar pain is the main symptom. Palmoplantar keratoderma and nail dystrophy are the predominant characteristics, often accompanied by oral leucokeratosis, cysts and follicular keratosis. What does this study add? This study identifies PC‐associated keratin mutations in 84 new families with PC recruited by the International Pachyonychia Congenita Research Registry. Fourteen of the 46 distinct keratin mutations were previously unreported. This study expands the large well‐phenotyped and genotyped case series of patients with PC, which is an invaluable resource for the development of mutation‐specific and/or gene‐specific therapies and for future clinical trials.