Severe Palmo-Plantar Hyperkeratosis in Koebner Epidermolysis Bullosa Simplex.

SHIRAKATA Y; TAMAI K; NAKAOKA H; TOKUMARU S; SAYAMA K; MURAKAMI S; HASHIMOTO K

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J-GLOBAL ID：200902296019627576 Reference number：03A0159492

Severe Palmo-Plantar Hyperkeratosis in Koebner Epidermolysis Bullosa Simplex.

Koebner単純型先天性表皮水ほう症における重度掌せき角化症

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Author (7)： , , , , , ,
Material：
Volume： 30 Issue： 2 Page： 135-140 Publication year： Feb. 2003
JST Material Number： Z0757A ISSN： 0385-2407 Document type： Article
Article type：短報 Country of issue： Japan (JPN) Language： ENGLISH (EN)

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Skin diseases

Reference (29)：

FINE, JD. Revised classification system for inherited epidermolysis bullosa : Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa. J Am Acad Dermatol. 2000, 42, 1051-1066
LETAI, A. Disease severity correlates with position of keratin point mutations in patients with epidermolysis bullosa simplex. Proc Natl Acad Sci USA. 1993, 90, 3197-3201
CHAN, YM. Mutations in the non-helical linker segment L1-2 of keratin 5 in patients with Weber-Cockayne epidermolysis bullosa simplex. J Cell Sci. 1994, 107, 765-774
BUCHBINDER, LH. Severe infantile epidermolysis bullosa simplex. Dowling-Meara type. Arch Dermatol. 1986, 122, 190-198
SHEMANKO, CS. Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14). J Invest Dermatol. 1998, 111, 893-895

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