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- ichthyosis nigricans 黑鱼鳞病
- Excessive or abnormal dryness of the skin,as in ichthyosis. 干皮病皮肤异常或不正常的干燥，如鱼鳞癣
- Excessive or abnormal dryness of the skin, as in ichthyosis. 干皮病皮肤异常或不正常的干燥，如鱼鳞癣
- A 9 years old boy with X-linked ichthyosis is reported. 报告1例伴房间隔缺损的X-连锁鱼鳞病。
- Skin biopsy showed a typical characteristic of acanthosis nigricans. 皮损有典型的组织病理改变,血清胰岛素、睾酮水平升高。
- Objective: To investigate the clinical feature of obese acanthosis nigricans. 摘要目的：探讨肥胖性黑棘皮病的临床特点。
- Objective:To investigate the clinical feature of obese acanthosis nigricans. 目的:探讨肥胖性黑棘皮病的临床特点。
- Harlequin ichthyosis （HI）is a severe subtype of autosomal recessive congenital ichthyoses (ARCI). 丑角样鱼鳞病是常染色体隐性遗传性鱼鳞病的一种严重亚型。
- Any of various rot-causing fungi of the genus Rhizopus, such as R. nigricans, the common bread mold. 根霉任一种根霉属属类中的各种致腐真菌中，例如黑根霉即普通的面包霉菌
- Keratitis, ichthyosis, and deafness syndrome (KID syndrome) is a rare congenital disorder disease. 目的观察角膜炎、鱼鳞病、耳聋综合征的临床表现。
- In patch and plaque stage, MF may resemble eczema, psoriasis, pityriasis rubra pilaris, ichthyosis and etc. 但肿瘤前期MF临床表现无特异性，可类似湿疹、银屑病、毛发红糠疹、鱼鳞病等，而红皮病型MF也易与上述疾病引起的红皮病相混淆，所以对疑似病例有必要行皮肤活检等相关检查。
- Conclusion Two cases of epidermolytic hyperkeratosis ichthyosis may result from spontaneous mutation. 结论2例表皮松解性角化过度鱼鳞病可能由自发突变引起。
- Preclinical progress has been achieved in the treatment of wounds, epidermolysis bullosa and ichthyosis. 前期的临床实验在治疗创伤，大疱性表皮松解症和鱼鳞病上已经取得了进展.
- The ITS sequence can be used as identification method for R. subnigricans and R. nigricans. ITS序列分析方法可以作为两者的鉴定方法。
- Ichthyosis broke the myth can not be cured, medical history can be called one of the greatest achievements. 打破了鱼鳞病不能治愈的神话，堪称医学史上最伟大的成就之一。
- Objective To explore the high risk factors of metabolic syndrome(MS) in obese children with acanthosis nigricans. 目的探讨肥胖伴黑棘皮病儿童代谢综合征(MS)的高危因素。
- We herein report a case of harlequin ichthyosis, which we believe is the first such case in Taiwan. 本文报告台湾第一宗丑角性鱼鳞癣之病例，并回顾文献其临床特征，处理与预后做进一步探讨。
- It was also found that the percentage of T8~+ cell in AD patients with respiratory allergy and ichthyosis was significantly reduced. AD患者血清IgE显著高于正常人,但与T_8~+细胞低下无相关性。
- Sjogren-Larsson syndrome (or Rud's syndrome) is a form of ichthyosis associated with a deficiency of the enzyme "fatty aldehyde dehydrogenase". 什么是'干燥，拉尔森综合征-罕见的遗传疾病与皮肤增厚'?
- A case of 14-year-old female with hyperandrogenism, insulin resistance and acanthosis nigricans (HAIR-AN) syndrome is reported. 报告1例高雄激素血症-胰岛素抵抗-黑棘皮病综合征。
