Ichthyosis associated with ARC syndrome: ARC syndrome is one of the differential diagnoses of ichthyosis

被引:9
作者
Choi, HJ [1 ]
Lee, MW [1 ]
Choi, JH [1 ]
Moon, KC [1 ]
Koh, JK [1 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Dermatol, Seoul 138736, South Korea
关键词
D O I
10.1111/j.1525-1470.2005.00135.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
The arthrogryposis, renal tubular dysfunction and cholestasis syndrome is rare. Novel identification of the mutation in VPS33B in this syndrome, which involves intracellular protein trafficking by regulation of vesicle-to-target sensory nerve action potential receptor (SNARE) family, might explain the consistent combination of membrane fusion defects. We can guess the defective lamellar body secretion mediated by the soluble N-ethylmaleimide-sensitive factor attachment protein receptor or SNARE protein pathway in the epidermis might result in the ichthyosiform phenotype. In the English-language literature, half of the reported instances of this syndrome are associated with ichthyosis. We report an infant with ichthyosis in association with arthrogryposis, renal tubular dysfunction, and cholestasis syndrome, and review the literature. Our findings suggest that the differential diagnosis of ichthyosis during infancy should include this syndrome.
引用
收藏
页码:539 / 542
页数:4
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