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Autosomal dominant lamellar ichthyosis: a new skin disorder

✍ Scribed by H. Traupe; G. Kolde; R. Happle


Book ID
119839626
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
460 KB
Volume
26
Category
Article
ISSN
0009-9163

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The association of X-linked ichthyosis with a deficiency of steroidsulfatase was demonstrated biochemically in cultured skin fibroblasts and epidermal cells in recent years [9,2]. A simultaneous deficiency of arylsulfatase C in this inborn error was shown histochemically in skin sections by Koppe et