Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations
Author:
Publisher
Elsevier BV
Subject
Dermatology,Molecular Biology,Biochemistry
Reference18 articles.
1. Steroid sulphatase deficiency disease;Lykkesfeldt;Clin Genet,1985
2. Pathogenesis of permeability barrier abnormalities in the ichthyoses: inherited disorders of lipid metabolism;Elias;J Lipid Res,2008
3. Ichthyosis of steroid sulphatase deficiency clinical study of 76 cases;Hoyer;Dermatologica,1986
4. Clinical spectrum of steroid sulfatase deficiency: X-linked recessive ichthyosis, birth complications and cryptorchidism;Traupe;Eur J Pediatr,1983
5. A clinical and genetic study of X-linked recessive ichthyosis and contiguous gene defects;Paige;Br J Dermatol,1994
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