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Hyperkeratosis‐hyperpigmentation syndrome: a confirmative case
Author(s) -
Figuera L. E.,
RodriguezCatellanos M. A.,
GonzalezMendoza A.,
Cantú J. M.
Publication year - 1993
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1993.tb04430.x
Subject(s) - dermatology , hyperkeratosis , hyperpigmentation , medicine , skin hyperpigmentation , dyskeratosis , ichthyosis , genetics , biology
A 22‐year‐old female showing hyperpigmented spots and mild palmoplantar hyperkeratosis as leading features is presented. The diagnosis of Hyperkeratosis‐hyperpigmentation syndrome, previously described by our group as an autosomal dominant trait, was unmistakable, thus permitting the corroboration of this genodermatosis.