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Variant of Keratoderma hereditaria mutilans (Vohwinkel's syndrome). Treatment with orally administered isotretinoin
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A missense mutation in connexim 26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families
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Functional defects in a family with deaf mutism and palmoplantar keratodermm
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A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome
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Maestrini E, Monaco AP, McGrath JA, Ishida-Yamamoto A, Camisa C, Hovnanian A, et al. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. Nat Genet 1996;13:70-7.
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Keratoderma hereditaria mutilans (Vohwinkel's syndrome) associated with congenital deaf mutism
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Peris K, Salvati EF, Torlone G, Chimenti S. Keratoderma hereditaria mutilans (Vohwinkel's syndrome) associated with congenital deaf mutism. Br J Dermatol 1995;132:617-20.
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Mutilating palmoplantar keratoderma successfully treated with etretinate
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Etretinate: Management of keratoma hereditaria mutilans in four family members
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