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- ichthyosis congenita 先天鳞癣
- 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
- 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。
- Conclusion(s): Aplasia cutis congenita is easily ignored when the lesion is small. 当先天性表皮发育不全伤口面积很小时，极易被忽略。
- We report this case and also review the literature, and then we suggest a checklist for aplasia cutis congenita. 我们报告此一病例，并整理文献列出一个清单，用以处理先天性表皮发育不全之作业流程。
- A case of dyskeratosis congenita is reported and the family pedigree is also analyzed. 报告1例先天性角化不良并附家系调查报告。
- 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。
- Skin biopsy was obtained from five cases,revealing pathological changes consistent with dyskeratosis congenita. 5例患者的皮损曾行组织病理学检查,其改变均与本病相符。
- 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。
- A hereditary form, myotonia congenita (Thomsen's disease), can affect eyelid and eye motion, swallowing, or talking. 具遗传性的先天性肌强直（汤姆生氏病），会影响眼睑和眼睛的运动、吞咽或说话。
- 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.
- Objective: As shown in published literatures, aplasia cutis congenita (ACC) is an uncommon anomaly among newborns and is often overlooked when the lesion is small. 摘要目的：先天性表皮发育不全为一种少见的先天性疾病，但往往因为缺损体积过小而被忽略。
- 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。
- 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。
- There is an association with other abnormalities in at least 50% of the patients with cutis marmorata telangiectatica congenita. 本文所报告的病例乃是一位三十八天大的女婴儿，出生时即有此皮肤病兆。
- As shown in published literatures, aplasia cutis congenita (ACC) is an uncommon anomaly among newborns and is often overlooked when the lesion is small. 摘要目的：先天性表皮发育不全为一种少见的先天性疾病，但往往因为缺损体积过小而被忽略。
- 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。
