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Quoted phrase not found in phrase index: "Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome"
Page 1
Cutaneous paraneoplasia.
Ramos-E-Silva M, Carvalho JC, Carneiro SC. Ramos-E-Silva M, et al. Clin Dermatol. 2011 Sep-Oct;29(5):541-7. doi: 10.1016/j.clindermatol.2010.09.022. Clin Dermatol. 2011. PMID: 21855730
This contribution presents the morphologic aspects and the differential diagnosis of the main paraneoplasias, which include acanthosis nigricans, tripe palms, Leser-Trelat sign, acquired ichthyosis, acquired hypertrichosis lanuginosa, pityriasis rotunda, erythema gyratum repens, …
This contribution presents the morphologic aspects and the differential diagnosis of the main paraneoplasias, which include acanthosis nigri …
Diagnosis and Management of Inherited Palmoplantar Keratodermas.
Thomas BR, O'Toole EA. Thomas BR, et al. Acta Derm Venereol. 2020 Mar 25;100(7):adv00094. doi: 10.2340/00015555-3430. Acta Derm Venereol. 2020. PMID: 32147745 Free PMC article. Review.
Palmoplantar keratodermas are grouped depending on the morphology of the keratoderma into diffuse, focal/striate or papular/punctate. Some palmoplantar keratodermas just affect the skin of the palms and soles and others have associated syndromic featur …
Palmoplantar keratodermas are grouped depending on the morphology of the keratoderma into diffuse, focal/striate or papular/pu …
Keratitis-ichthyosis-deafness (KID) syndrome.
Gonzalez ME, Tlougan BE, Price HN, Patel R, Kamino H, Schaffer JV. Gonzalez ME, et al. Dermatol Online J. 2009 Aug 15;15(8):11. Dermatol Online J. 2009. PMID: 19891919 Free article.
A 21-year-old man presented with a life-long history of diffusely thickened skin with a grainy-to-ridged surface, verrucous perioral plaques with radial fissures, and diffuse palmoplantar keratoderma with a stippled appearance. These skin findings were accompanied by senso …
A 21-year-old man presented with a life-long history of diffusely thickened skin with a grainy-to-ridged surface, verrucous perioral plaques …
Palmoplantar keratodermas: clinical and genetic aspects.
Has C, Technau-Hafsi K. Has C, et al. J Dtsch Dermatol Ges. 2016 Feb;14(2):123-39; quiz 140. doi: 10.1111/ddg.12930. J Dtsch Dermatol Ges. 2016. PMID: 26819106 Review.
Palmoplantar keratodermas comprise a diverse group of acquired and hereditary disorders marked by excessive thickening of the epidermis of palms and soles. Early onset and positive family history suggest a genetic cause. While hereditary forms of palmoplantar keratoderm …
Palmoplantar keratodermas comprise a diverse group of acquired and hereditary disorders marked by excessive thickening of the epiderm …
Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype-phenotype correlation.
Ennouri M, Zimmer AD, Bahloul E, Chaabouni R, Marrakchi S, Turki H, Fakhfakh F, Bougacha-Elleuch N, Fischer J. Ennouri M, et al. BMC Med Genomics. 2022 Jan 5;15(1):4. doi: 10.1186/s12920-021-01154-z. BMC Med Genomics. 2022. PMID: 34983512 Free PMC article.
BACKGROUND: Ichthyosis is a heterogeneous group of Mendelian cornification disorders that includes syndromic and non-syndromic forms. Autosomal Recessive Congenital Ichthyosis (ARCI) and Ichthyosis Linearis Circumflexa (ILC) belong to non-syndromic forms. …
BACKGROUND: Ichthyosis is a heterogeneous group of Mendelian cornification disorders that includes syndromic and non-syndromic …
Papillon-Lefevre syndrome.
Landow RK, Cheung H, Bauer M. Landow RK, et al. Int J Dermatol. 1983 Apr;22(3):177-9. doi: 10.1111/j.1365-4362.1983.tb03359.x. Int J Dermatol. 1983. PMID: 6222004
A patient, with Papillon-Lefevre syndrome, presented with a premature loss of both deciduous and permanent teeth and hyperkeratosis palmaris et plantaris. ...
A patient, with Papillon-Lefevre syndrome, presented with a premature loss of both deciduous and permanent teeth and hyperkeratosis p …
Cell-cell connectivity: desmosomes and disease.
Brooke MA, Nitoiu D, Kelsell DP. Brooke MA, et al. J Pathol. 2012 Jan;226(2):158-71. doi: 10.1002/path.3027. Epub 2011 Nov 14. J Pathol. 2012. PMID: 21989576 Review.
A broad spectrum of inherited, infectious and auto-immune diseases can affect the proper function of intercellular junctions and result in either diseases affecting specific individual tissues or widespread syndromic conditions. A particularly diverse group of diseases res …
A broad spectrum of inherited, infectious and auto-immune diseases can affect the proper function of intercellular junctions and result in e …
Molecular Genetics of Keratinization Disorders - What's New About Ichthyosis.
Uitto J, Youssefian L, Saeidian AH, Vahidnezhad H. Uitto J, et al. Acta Derm Venereol. 2020 Mar 25;100(7):adv00095. doi: 10.2340/00015555-3431. Acta Derm Venereol. 2020. PMID: 32147742 Free PMC article. Review.
The heritable forms of keratinization disorders, including various forms of ichthyosis and keratodermas, comprise a phenotypically heterogeneous group of diseases which can be divided into syndromic and non-syndromic forms. In the non-syndromic forms, …
The heritable forms of keratinization disorders, including various forms of ichthyosis and keratodermas, comprise a phenotypically he …
Retinoids in disorders of keratinization: their use in adults.
Happle R, van de Kerkhof PC, Traupe H. Happle R, et al. Dermatologica. 1987;175 Suppl 1:107-24. doi: 10.1159/000248867. Dermatologica. 1987. PMID: 2961628 Review.
Good or excellent results have been seen in other forms of palmoplantar keratoderma including mal de Meleda, Papillon-Lefevre syndrome, erythrokeratodermia variabilis, verrucous epidermal nevi, Darier disease and pityriasis rubra pilaris. In patients with Darier dis …
Good or excellent results have been seen in other forms of palmoplantar keratoderma including mal de Meleda, Papillon-Lefevre synd …
Prevalence and treatment of palmoplantar keratoderma and tinea pedis in patients with Sezary syndrome.
Martin SJ, Duvic M. Martin SJ, et al. Int J Dermatol. 2012 Oct;51(10):1195-8. doi: 10.1111/j.1365-4632.2011.05204.x. Int J Dermatol. 2012. PMID: 22994666
Sezary syndrome is characterized by blood involvement, exfoliative eryrthroderma, lymphadenopathy, pruritus, keratoderma, and immunosuppression. ...CONCLUSIONS: The prevalence of palmoplantar keratoderma in Sezary syndrome is 61.6%, with co-existing ti …
Sezary syndrome is characterized by blood involvement, exfoliative eryrthroderma, lymphadenopathy, pruritus, keratoderma, and …
82 results