ichthyosis

Objective To study the nursing experience of children with severe ichthyosis .

目的探讨重症鱼鳞病患儿的临床护理经验。

Serum essential fatty acid analyses in patients with psoriasis and ichthyosis

银屑病和鱼鳞病患者血清必需脂肪酸分析

Keratitis ichthyosis and deafness syndrome : first report in China

角膜炎·鱼鳞病·耳聋综合征&国内首例报告

Analysis on the Genotype and Clinical Phenotype Correlations of Four Style Heritage Ichthyosis

四种遗传性鱼鳞病基因型与临床表型的相关性分析

First report of gene mutation in a Chinese patient with ichthyosis bullosa of Siemens

Siemens大疱性鱼鳞病基因突变国内首次报道

Nursing for 23 children with severe ichthyosis

重症鱼鳞病患儿的护理23例

Objective To identify gene mutations of two cases of epidermolytic hyperkeratosis ichthyosis .

目的研究二例表皮松解性角化过度型鱼鳞病患者基因突变情况。

Ichthyosis bullosa of Siemens : Its correct diagnosis facilitated by molecular genetic testing

分子遗传学检测使Siemens大疱性鱼鳞病易于正确诊断

Pathological observation of ichthyosis hystrix Lambert type with light and electron microscopes

Lambert型豪猪状鱼鳞病的光镜及电镜分析

Double blind randomized controlled clinical trial of lactic acid compound ointment in the treatment of ichthyosis vulgaris

复方乳酸软膏治疗寻常型鱼鳞病随机双盲基质对照多中心临床研究

Transglutaminase 1 gene mutations in a family with lamellar ichthyosis

板层状鱼鳞病TGM1基因突变研究

Gene Mutations in Two Sporadic Cases of Epidermolytic Hyperkeratosis Ichthyosis

表皮松解性角化过度型鱼鳞病二例及其基因突变的研究

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。

Ocular manifestations of keratitis - ichthyosis - deafness ( KID ) syndrome

角膜炎-鱼鳞癣-耳聋（KID）综合征的眼部表现

Investigation of STS Gene in a Pedigree with X-Linked Ichthyosis

X性联锁遗传鱼鳞病一家系的STS基因研究

Barrier dysfunction and pathogenesis of neutral lipid storage disease with ichthyosis ( Chanarin-Dorfman syndrome )

伴鱼鳞病的中性脂质贮存异常的发病机制和屏障功能障碍（Chanarin-Dorfman综合征）

Fishskin disease Expressions of genes associated with growth and differentiation in peripheral blood leukocytes of lamellar ichthyosis patients

板层状鱼鳞病患者外周血白细胞生长、分化相关基因的表达

Ultrastructural alterations of the stratum corneum lipids in patients with lamellar ichthyosis

板层状鱼鳞癣病人角质层脂质超微结构的观察

But doctors have told the family there is still no known cure for the genetic condition , known as Lamellar ichthyosis .

小宋胜得的病被称为层状鱼鳞病，然而，医生们告诉小宋胜的家人，他们没有此类基因病的有效治愈方法。

Q & A on Sex Epidermolytic hyperkeratosis ichthyosis complicated by dwarf : a case report

表皮松解性角化过度鱼鳞病伴侏儒1例

OBJECTIVE : To evaluate the efficacy and safety of urea & lactic acid compound ointment for the treatment of ichthyosis vulgaris .

前言：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。

A case of X-linked ichthyosis with interatrial septal defect

伴房间隔缺损的X-连锁鱼鳞病1例

Prenatal exclusion of harlequin ichthyosis ; potential pitfalls in the timing of the fetal skin biopsy

产前排除丑角样鱼鳞病：择时胎儿皮肤活检的潜在缺陷

Objective To elucidate the pathogenic genes in a pedigree with autosomal dominant ichthyosis vulgaris ( IV ) .

目的研究一常染色体显性遗传寻常型鱼鳞病家系的致病基因。

Ethnic Difference in Osteoporosis Related Phenotypes and Its Potential Underlying Genetic Determination ; Analysis on the Genotype and Clinical Phenotype Correlations of Four Style Heritage Ichthyosis

骨质疏松症相关表型的种族差异及其相关遗传决定的研究四种遗传性鱼鳞病基因型与临床表型的相关性分析

Objective To detect the mutations of transglutaminase 1 ( TGM1 ) gene in a family with lamellar ichthyosis .

目的探讨一个板层状鱼鳞病家系转谷氨酰胺酶1基因（TGM1）的突变。

We studied disseminated superficial actinic porokeratosis ( DSAP ) and ichthyosis vulgaris ( IV ) .

我们研究了播散性浅表光化性汗孔角化症（DSAP）和寻常型鱼鳞病（IV）。

The patients with DSH in family ⅳ were also affected by ichthyosis vulgaris . Patients with DSH in other families were not affected by other diseases .

除家系Ⅳ患者同患寻常型鱼鳞病以外，其它家系基本不伴发其他疾病。

The diagnosis was ichthyosis in histopathological examination , congenital nerve deaf-mutism in otolaryngology and corneal pannus in ophthalmology .

躯干部皮肤明显干燥，皮肤角化过度，呈皮革样变化。病理活检为鱼鳞病，耳科检查为先天感音神经性耳聋，眼科检查为角膜血管翳。

Diagnosing X-linked Ichthyosis by Monoplast Single-round Duplex PCR

单细胞单轮二重PCR诊断X-连锁鱼鳞病