ichthyosis

On admission he was found to have widespread congenital ichthyosis.

入院时发现,其身体多处患有先天性鳞癣,热度已消,但颈部、下和腹股沟淋巴腺仍肿大,脾缘可触及.

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。

Objective To detect the mutations of GJB2 and GJB6 genes in the first Chinese case of keratitis, ichthyosis and deafness ( KID) syndrome.

目的检测国内首例先天性角膜炎、鱼鳞病、耳聋综合征（KID）患者的GJB2基因和GJB6基因突变。

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。

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

Nursing for 23 children with severe ichthyosis

重症鱼鳞病患儿的护理23例

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.

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.

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.

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

Results: 97 cases were randomly divided into three groups. After 28 days treatment, respectively the efficacy rates were 100%, 100% for ichthyosis vulgaris and rhagadia manus and pedalis in test group, vs.

结果：97例患者随机分为试验组、对照组和开放组，28d治疗后，试验组鱼鳞病和手足皲裂的有效率均为100%、对照组则分别为91.7%和27.3%。

Transglutaminase 1 gene mutations in a family with lamellar ichthyosis

板层状鱼鳞病TGM1基因突变研究

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）

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

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

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

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.

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。

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

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）。

OBJECTIVE: To study retrospectively the effect and ADRs of etretinate in 49 patients of keratinization, including psoriasis 33 cases, pityriasis rubra pilaris 6 cases, ichthyosis 3 cases and lichen planus 7 cases.

目的：回顾性研究了依曲替酯治疗49例角化性疾病（银屑病33例，毛发红糠疹6例，鱼鳞病3例和扁平苔藓7例）的疗效及不良反应等。

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

Objective To detect the activity of transglutaminase 1 ( TGM 1 ) and gene mutation in a family with lamellar ichthyosis.

目的检测一板层状鱼鳞病家系中患者转谷氨酰胺酶1的活性及其编码基因的突变.

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

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

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。

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

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

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