Ichthyosiform erythroderma
ichthyosiform erythroderma ich·thy·o·si·form erythroderma (ĭk’thē-ō’sə-fôrm’)
n.
Variant of congenital ichthyosiform erythroderma.
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[ik-thee-oh-sis] /ˌɪk θiˈoʊ sɪs/ noun, Pathology. 1. a hereditary skin disease in which the epidermis continuously flakes off in large scales or plates. /ˌɪkθɪˈəʊsɪs/ noun 1. a congenital disease in which the skin is coarse, dry, and scaly Also called xeroderma Nontechnical name fishskin disease n. 1815, Modern Latin, from Greek ikhthys “fish” + -osis. […]
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ichthyosis linearis circumscripta ichthyosis lin·e·ar·is cir·cum·scrip·ta (lĭn’ē-âr’ĭs sûr’kəm-skrĭp’tə) n. An inherited skin disorder present at birth or appearing in infancy, characterized by redness and scaling that moves from place to place about the body and shows a peripheral double-edged scale.
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ichthyosis sauroderma ichthyosis sau·ro·der·ma (sôr’ə-dûr’mə) n. See ichthyosis.
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ichthyosis simplex ichthyosis sim·plex (sĭm’plěks’) n. See ichthyosis vulgaris.
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ichthyosis uteri ichthyosis u·ter·i (yōō’tə-rī’) n. The transformation of the columnar epithelium of the endometrium into stratified squamous epithelium.