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- ichthyosis fetalis 胎儿鱼鳞病
- 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。
- Methods:To analyze clinical data of 68 cases of hydrops fetalis. 方法:结合68例水肿胎的临床资料进行分析。
- Results:The mortality rate of hydrops fetalis was bally high (100%) . 结果:水肿胎死亡率为100.;00%25。
- Blood typing also helps identify disorders such as erythroblastosis fetalis. 此外,血型分类还可以帮助诊断某些疾病,如胎儿母红血球增多症。
- 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。
- The epidemic trend and preventive strategy of Hb Bart hydrops fetalis sequence from 1998 to 2003 in Guangdong province. 巴氏水肿胎儿序列征流行趋势及干预对策
- The pathophysiology and management of the complications of hydrops fetalis with chorioangioma are discussed. 本篇讨论此病所产生之并发症，其病理生理及处理之原则。
- 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.
- Chorioangioma is the most common tumor of the placenta.However, a large one complicated with hydrops fetalis is rare. 摘要绒毛膜血管瘤虽为胎盘常见的肿瘤之一，但其中合并胎儿水肿者仍是少数。
- 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。
- 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'?
- OBJECTIVE:To evaluate the efficacy and safety of urea &lactic acid compound ointment for the treatment of ichthyosis vulgaris. 目的:评价尿素乳酸软膏治疗寻常型鱼鳞病的有效性和安全性。
