| [1] Herna′ndez-Mart?′n A, Gonza′lez-Sarmiento R, De Unamuno P.X-linked ichthyosis: an update. Br J Dermatol,1999,141:617-627. [2] Valdes M, Kofman SH, Vaca AL, et al. Mutation report: a novel partial deletion of exons 2-10 of the STS gene in recessive X-linked ichthyosis. J Invest Dermatol, 2000, 114(3): 591-593. [3] Thauvin-Robinet C, Lambert D, Vaillant G, et al. X-linked recessive ichthyosis in a girl: strategy for identifying the causal mechanism. Br J Dermatol,2005,152:191-193. [4] Elias PM，Cmmrine D，Rassner U，et a1．Basis for abnormal desquamation and permeability barrier dysfunction in RXLI．J Invest Dermatol,2004，122：314． [5] Fernandes NF, Janniger CK, Schwartz RA.X-linked ichthyosis: an oculocutaneous genodermatosis.J Am Acad Dermatol，2010，62(3):480-485. [6] 孙秀坤，朱学骏.先天性鱼鳞病致病基因的研.临床皮肤科杂志,2003,32(11):690-692. [7] Kent L, Emerton J, Bhadravathi V, et a1．X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits．J Med Genet，2008，45(8):519-524. |
