Erythrokeratoderma: a manifestation associated with multiple types of ichthyoses with different gene defects

被引：10
|
作者：
Youssefian, L. [1 ,2 ]
Touati, A. [1 ,4 ]
Vahidnezhad, H. [1 ,5 ]
Saeidian, A. H. [1 ]
Sotoudeh, S. [3 ]
Zeinali, S. [5 ,6 ]
Uitto, J. [1 ]
机构：
[1] Thomas Jefferson Univ, Dept Dermatol & Cutaneous Biol, Sidney Kimmel Med Coll, Philadelphia, PA 19107 USA
[2] Univ Tehran Med Sci, Dept Med Genet, Sch Med, Tehran, Iran
[3] Univ Tehran Med Sci, Childrens Med Ctr, Ctr Excellence, Dept Dermatol, Tehran, Iran
[4] Drexel Univ, Coll Med, Philadelphia, PA 19104 USA
[5] Pasteur Inst Iran, Dept Mol Med, Biotechnol Res Ctr, Tehran, Iran
[6] Kawsar Human Genet Res Ctr, Tehran, Iran
来源：
BRITISH JOURNAL OF DERMATOLOGY | 2018年 / 178卷 / 03期
关键词：
PROGRESSIVE SYMMETRIC ERYTHROKERATODERMA; RECESSIVE CONGENITAL ICHTHYOSIS; PHENOTYPIC SPECTRUM; MUTATION; VARIABILIS;
D O I：
10.1111/bjd.16053
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
引用
收藏
页码：E219 / E221
页数：3
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