ichthyosis的例句大全

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

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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

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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

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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

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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。

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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。

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these vary in size, some being fine, delicate, and branny, as in eczema and ichthyosis, while still others are stratified, as in psoriasis.

鳞屑大小不一，有的细小如糠状，如湿疹和鱼鳞病的鳞屑；还有的成层状，如银屑病的鳞屑。

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this disease is characterized by limb length discrepancies, growth retardation, ichthyosis, cataracts, and punctate calcification.

这种疾病的特点是下肢长度差异，生长迟缓，鱼鳞病，白内障，和点状钙化。

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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

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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.

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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.

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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.

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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.

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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.

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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.

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