Results 71 to 80 of about 171 (84)
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Clinical and Experimental Dermatology, 2009
We report a patient of Malay ancestry with dermatopathia pigmentosa reticularis (DPR) resulting from a recurrent KRT14 p.R125C mutation. The patient has reticulate hyperpigmentation over his trunk and proximal limbs, together with onychodystrophy.
B K, Goh +3 more
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We report a patient of Malay ancestry with dermatopathia pigmentosa reticularis (DPR) resulting from a recurrent KRT14 p.R125C mutation. The patient has reticulate hyperpigmentation over his trunk and proximal limbs, together with onychodystrophy.
B K, Goh +3 more
openaire +2 more sources
British Journal of Dermatology
Abstract The KRT14 gene is 4615 base pairs long and has eight exons. It encodes the intermediate filament protein keratin 14, which is 472 amino acids long and has four helical domains flanked by a nonhelical head domain and tail domain.
Schaida Schirwani, Mira Kharbanda
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Abstract The KRT14 gene is 4615 base pairs long and has eight exons. It encodes the intermediate filament protein keratin 14, which is 472 amino acids long and has four helical domains flanked by a nonhelical head domain and tail domain.
Schaida Schirwani, Mira Kharbanda
openaire +1 more source
Dermatopathia pigmentosa reticularis hyperkeratotica et mutilans
Dermatologica, 2009openaire +2 more sources
[Dermatopathia pigmentosa reticularis].
Annales de dermatologie et de venereologie, 2015S, Gallouj +5 more
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[The concept dermatopathia pigmentosa reticularis].
Zeitschrift fur Hautkrankheiten, 1974M, Lunder, J, Jettich
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Dermatopathia pigmentosa reticularis with beard alopecia: first report from Syria
Oxford Medical Case Reports, 2020exaly