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An Unusual Case of Palmoplantar Keratoderma—Diagnosis

Arch Dermatol. 2010;146(12):1419-1424. doi:10.1001/archdermatol.2010.357-b.
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REFERENCES
Huriez  CDeminatti  MAgache  PMennecier  M A gene dysplasia not previously known: frequently degenerative sclero-atrophying and keratodermic genodermatosis of the extremities [in French]. Sem Hop 1968;44 (8) 481- 488
PubMed
Patrizi  ADi Lernia  VPatrone  P Palmoplantar keratoderma with sclerodactyly (Huriez syndrome). J Am Acad Dermatol 1992;26 (5, pt 2) 855- 857
PubMed Link to Article[[XSLOpenURL/10.1016/0190-9622(92)70121-U]]
Kavanagh  GMJardine  PEPeachey  RDMurray  JCDe Berker  D The scleroatrophic syndrome of Huriez. Br J Dermatol 1997;137 (1) 114- 118
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Hamm  HTraupe  HBröcker  EBSchubert  HKolde  G The scleroatrophic syndrome of Huriez: a cancer-prone genodermatosis. Br J Dermatol 1996;134 (3) 512- 518
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Delaporte  EN’guyen-Mailfer  CJanin  A  et al.  Keratoderma with scleroatrophy of the extremities or sclerotylosis (Huriez syndrome): a reappraisal. Br J Dermatol 1995;133 (3) 409- 416
PubMed Link to Article[[XSLOpenURL/10.1111/bjd.1995.133.issue-3]]
Lee  Y-AStevens  HPDelaporte  EWahn  UReis  A A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23. Am J Hum Genet 2000;66 (1) 326- 330
PubMed Link to Article[[XSLOpenURL/10.1086/302718]]
Guerriero  CAlbanesi  CGirolomoni  G  et al.  Huriez syndrome: case report with a detailed analysis of skin dendritic cells. Br J Dermatol 2000;143 (5) 1091- 1096
PubMed Link to Article[[XSLOpenURL/10.1046/j.1365-2133.2000.03793.x]]
Watanabe  ETakai  TIchihashi  MUeda  M A nonfamilial Japanese case of Huriez syndrome: p53 expression in squamous cell carcinoma. Dermatology 2003;207 (1) 82- 84
PubMed Link to Article[[XSLOpenURL/10.1159/000070951]]
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