AnatomyDiseasesChemicals and DrugsAnalytical, Diagnostic and Therapeutic Techniques and EquipmentPhenomena and ProcessesHealth Care
IchthyosisIchthyosis, LamellarIchthyosis VulgarisIchthyosis, X-LinkedIchthyosiform Erythroderma, CongenitalSteryl-SulfataseHyperkeratosis, EpidermolyticArylsulfatasesKeratolytic AgentsIchthyosis Bullosa of SiemensKeratin-2PhotophobiaTransglutaminasesSjogren-Larsson SyndromeKeratin-1SulfatasesHypotrichosisGenes, RecessiveEctropionAcitretinEpidermisKeratoderma, PalmoplantarKeratin-10EmollientsLipid Metabolism, Inborn ErrorsIntermediate Filament ProteinsSkin Diseases, GeneticSkinEtretinateConsanguinityPelger-Huet Anomaly1-Acylglycerol-3-Phosphate O-AcyltransferaseSkin Diseases, VesiculobullousKeratinocytesPycnodysostosisArachidonate 12-LipoxygenasePedigreeDermatitis, ExfoliativeMutationChondrodysplasia PunctataDermatologic AgentsNetherton SyndromeCystatin MX ChromosomePhenotypeFomites

Congenital ichthyosis: an overview of current and emerging therapies. (65/179)

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Pathogenesis of permeability barrier abnormalities in the ichthyoses: inherited disorders of lipid metabolism. (66/179)

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Mutation G827R in matriptase causing autosomal recessive ichthyosis with hypotrichosis yields an inactive protease. (67/179)

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KID syndrome. (68/179)

KID syndrome is a rare congenital disorder characterized by keratitis, ichthyosis, and deafness. We have described a 4-year-old girl who is treated with bland emollients and topical keratolytics such as urea and surprisingly observed marked improvement in skin hyperkeratosis and palmoplantar keratoderma. We think that along with urgent ophthalmologic and otolaryngologic measures, simple topical therapies may improve skin condition in KID syndrome precluding the possible hazards of systemic retinoid therapy.  (+info)

The clinical and morphologic features of nonepidermolytic ichthyosis in the golden retriever. (69/179)

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Granulocytic nuclear differentiation of lamin B receptor-deficient mouse EPRO cells. (70/179)

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Mouse neutrophils lacking lamin B-receptor expression exhibit aberrant development and lack critical functional responses. (71/179)

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Histopathologic characterization of epidermolytic hyperkeratosis: a systematic review of histology from the National Registry for Ichthyosis and Related Skin Disorders. (72/179)

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