A case of ophiasis type of alopecia areata in a patient with ring chromosome 18 syndrome

KAGIMOTO Yoshiko; MIZUASHI Masato; KIKUCHI Katsuko; AIBA Setsuya

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J-GLOBAL ID：201402284193297420 Reference number：14A0788605

A case of ophiasis type of alopecia areata in a patient with ring chromosome 18 syndrome

環状染色体18症候群患者における蛇行状脱毛型円形脱毛症の症例

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Material：
Volume： 41 Issue： 6 Page： 559-560 Publication year： Jun. 2014
JST Material Number： W1578A ISSN： 0385-2407 Document type： Article
Article type：短報 Country of issue： Australia (AUS) Language： ENGLISH (EN)

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Clinical dermatology in general

Reference (5)：

Stankiewicz P, Brozek I, Helias-Rodzewicz Z et al. Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18. Am J Med Genet 2001; 101: 226-239.
Spreiz A, Guilherme RS, Castellan C et al. Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18. J Pediatr 2013; 163: 1174-1178.
Uchida IA, McRae KN, Ray M. Familial Short Arm Deficiency of Chromosome 18 Concomitant with Arhinencephaly and Alopecia Congenita. Am J Hum Genet 1965; 17: 410-419.
Shimomura Y, Agalliu D, Vonica A. APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex. Nature 2010; 464: 1043.
Martinez-Mir A, Zlotogorski A, Gordon D. Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata. Am J Hum Genet 2007; 80: 316-328.

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