PuSH - Publikationsserver des Helmholtz Zentrums München: Eight novel mutations confirm the role of AAGAB in punctate palmoplantar keratoderma type 1 (Buschke-Fischer-Brauer) and show broad phenotypic variability.

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Giehl, K.A.* ; Herzinger, T.* ; Wolff, H.* ; Sárdy, M.* ; von Braunmuehl, T.* ; Dekeule-Neer, V.* ; Sznajer, Y.* ; Tennstedt, D.* ; Boes, P.* ; Rapprich, S.* ; Wagner, N.* ; Betz, R.C.* ; Braun-Falco, M.* ; Strom, T.M. ; Ruzicka, T.* ; Eckstein, G.N.

Eight novel mutations confirm the role of AAGAB in punctate palmoplantar keratoderma type 1 (Buschke-Fischer-Brauer) and show broad phenotypic variability.

Acta Derm.-Venereol. 96, 468-472 (2016)

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Punctate palmoplantar keratoderma (PPKP1; Buschke-Fischer-Brauer) is a rare autosomal dominant inherited skin disease characterized by multiple hyperkeratotic papules involving the palms and soles. Mutations have been found at 2 loci, on chromosomes 15q22-15q24 and 8q24.13-8q24.21. We recently identified mutations in 3 families, in the AAGAB gene on 15q, which encodes the alpha- and gamma-adaptin-binding protein p34. The current study examined 14 additional families, comprising a total of 26 affected individuals and identified 8 novel mutations in 9 families. In one family a mutation representing a known SNP that was present only in the affected individuals was found, and in 4 other families, previously reported mutations were found (1, 2). These results confirm the role of AAGAB in PPKP1. Our findings suggest that there is no correlation with age, but with mechanical factors. No additional obvious genotype phenotype correlation was observed, even when comparing different types of mutations. Rather, identical genotypes presented a very broad interfamilial and intrafamilial variability of phenotypes.

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