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1. X染色体連鎖劣性魚鱗癬recessive x linked ichthyosis [show details]
…#308100), also called steroid sulfatase deficiency, is an X-linked recessive, nonsyndromic ichthyosis caused by deletions or mutations in the STS gene encoding the steroid sulfatase enzyme . Due to location …
2. ムコ多糖症：臨床的特徴および診断mucopolysaccharidoses clinical features and diagnosis [show details]
…galactosamine-6-sulfatase (GALNS), located at 16q24.3 . MPS IV B (MIM #253010) is due to beta-galactosidase (GLB1) deficiency. The clinical features result from accumulation of keratan sulfate and chondroitin-6-sulfate …
3. 変形性膝関節症のマネージメントmanagement of knee osteoarthritis [show details]
… pharmaceutical-grade chondroitin sulfate was found to be statistically superior to placebo and similar to celecoxib in reducing pain and improving function . Either chondroitin (800 mg), celecoxib (200 …
4. 先天性魚鱗癬の概要と分類overview and classification of the inherited ichthyoses [show details]
…and dystrophic nails. Multiple sulfatase deficiency (MIM #272200) is a rare autosomal recessive disorder caused by deficiency of all lysosomal and microsomal sulfatase enzymes . Infants present with features …
5. 変形性手関節症のマネージメントmanagement of hand osteoarthritis [show details]
…recommend glucosamine or chondroitin for the treatment of hand OA, but, because of the beneficial safety profile, we do not discourage patients who wish to try these substances. Chondroitin sulfate and glucosamine …