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symmetrical progressive erythrokeratoderma
A case of progressive and symmetric erythrokeratoderma in a 9-year-old boy is presented. The evidence for loricrin as a candidate gene for this disorder as well ...
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Mar 15, 2004 ... Progressive symmetric erythrokeratoderma (PSEK, Gottron's Syndrome) in a 10 year-old-boy is reported. The diagnosis was confirmed by ...
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Mar 15, 2004 ... A case of progressive symmetric erythrokeratoderma (PSEK) associated with symmetric syndactylism is being reported. The interesting feature ...
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The molecular pathology of progressive symmetric erythrokeratoderma: a frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope.
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A young boy with symmetric hyperkeratotic plaques: progressive symmetric erythrokeratoderma (PSEK). Arroyo MP. mp.arroyo@stanfordalumni.org ...
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Jul 1, 2011 ... Progressive partially symmetrical erythrokeratoderma results in deafness, muscle weakness, peripheral nerve damage, physical and mental ...
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Progressive symmetric erythrokeratoderma (PSEK; OMIM 602036) is one of the less prevalent erythrokeratoderma variants initially described byGottron (1922).
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(1997) Ishida-Yamamoto et al. The American Journal of Human Genetics. Read by researchers in: 100% Biological Sciences. The erythrokeratodermas (EKs) ...
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Symmetrical progressive erythrokeratoderma is an autosomal dominant disorder.
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Oct 20, 2010 ... Progressive symmetric erythrokeratoderma (PSEK) is a rare genetic skin disorder characterized by well-demarcated plaques of reddened, dry, ...
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Did you mean:
symmetrical progressive erythrokeratoderma
