Objective To analyze genetic types and clinical features with anhidrotic ectodermal dysplasia ( EDA). 目的分析无汗性外胚叶发育不全的遗传类型和临床特点。
The inner ear, which mediates hearing and equilibrium, develops from an ectodermal placode located adjacent to the developing hindbrain. 内耳是调节听力和平衡的器官,来源于外胚层邻近后脑的生长板。
Prognostic factors of primitive neuroectodermal tumor Research progress in the genes and proteins of hypohidrosis ectodermal dysplasia 原始神经外胚层肿瘤化疗患者预后的研究少汗型外胚层发育不良症相关基因及其蛋白
Analysis of saliva from the patients with hypohidrotic ectodermal dysplasia 少汗型外胚层发育不良症患者全唾液分析
Clinical and genetic features of ectrodactyly, ectodermal dysplasia and clefting syndrome congenital absence of fingers and/ or toes. 先天性缺指(趾)-外胚叶发育不全-唇/腭裂综合征的临床和遗传学特点先天缺少手指或脚趾。
Oral rehabilitation nursing for patients with congenital ectodermal dysplasia 先天性外胚叶发育不全的口腔修复护理
ABSTRACT: Objective To identify the mutations of ED1 gene in a family with X-linked hypohidrotic ectodermal dysplasia. 摘要:目的利用直接测序法对一中国汉族人X性连锁少汗性外胚叶发育不良家系进行基因诊断。
Similar sequential and reciprocal interactions between the epithelium and mesenchyme regulate the early steps of development in all ectodermal organs. 上皮-间充质间相互作用在所有的外胚层来源的器官的发育早期均起到重要的调节作用。
Comparison of Sevoflurane and Ketamine used as Basal Anesthesia in Infants 'Primary Repair of Cleft Lip or/ and Palate Clinical and genetic features of ectrodactyly, ectodermal dysplasia and clefting syndrome 七氟醚与氯胺酮做基础麻醉在婴幼儿先天性唇腭裂手术中的应用比较先天性缺指(趾)-外胚叶发育不全-唇/腭裂综合征的临床和遗传学特点
Gene Diagnosis in a Family of Hidrotic Ectodermal Dysplasia 基因诊断有汗性外胚叶发育不良一家系
We derived cell populations with properties of ectodermal and mesenchymal cells in2D culture and incorporated these divergent cell populations into3D epithelial tissues. 我们利用二维培养将胚胎干细胞分化为具有外胚和间充质特性的细胞,再将这些细胞复合入三维上皮组织。
Objetive: To detect the gene mutation of a patient with anhidrotic ectodermal dysplasia. 目的:检测无汗性外胚层发育不全患者的EDA基因的突变。
A clinical and laboratory study on a case of hypohidrotic ectodermal dysplasia ( HED) accompanied by oligodontia HED伴多数牙先天缺失1例的临床研究
Objective To detect ED1 gene mutations in the families with X-linked hypohidrotic ectodermal dysplasia ( XLHED). 目的探讨X性连锁少汗性外胚层发育不良(XLHED)家系中ED1基因突变。
Objective To report the first case of ectodermal dysplasia/ skin fragility syndrome in China. 目的报道我国首例外胚层发育不良/皮肤脆性综合征。
This article reports a case of anhidrotic ectodermal dysplasia associated with giant type granuloma annulare. 报告1例无汗性外胚叶发育不良伴巨大型环状肉芽肿。
Ectodermal dysplasia showing clinical overlap between AEC, Rapp-Hodgkin and CHAND syndromes 外胚层发育不良症临床症状表现为AEC、Rapp-Hodgkin和CHAND综合征
Prenatal diagnosis of X-linked anhidrotic ectodermal dysplasia with X-chromosome inversion X染色体倒位伴X连锁无汗性外胚叶发育不良一个家系的产前诊断
A Pedigree Study on Congenital Hidrotic Ectodermal Dysplasia 一个先天性有汗性外胚层发育不良家系的调查研究
Congenital hidrotic ectodermal dysplasia: clinical and genetic features 有汗性外胚层发育不良临床及遗传特点分析
Ocular symptoms and signs in patients with ectodermal dysplasia syndromes 外胚层发育不良综合征患者的眼部症状和表现
Anhidrotic ectodermal dysplasia with spontaneous corneal perforation and keratoconus 无汗性外胚层发育不良伴特发性角膜穿孔和圆锥角膜的病例
Inductive interactions mediated by the Msx genes are essential for normal craniofacial, limb and ectodermal organ morphogenesis as manifested by the phenotypic abnormalities shown in knockout mice and in humans. 基因敲除鼠和人类的畸形表现型的研究显示,Msx基因介导的诱导组织间的相互作用,对正常颅颌面、肢体和外胚层器官的形态发生至关重要。
RESULTS: The patient was diagnosed as X-linked hypohidrotic ectodermal dysplasia. 结果:确证该患者是X染色体隐性遗传的外胚层发育不全无汗综合征;
Gene Mutation Analysis in Chinese Patients with Ectodermal Dysplasia 外胚层发育不良的基因突变研究
Histopathological and ultrastructural study of ectodermal dysplasia/ skin fragility syndrome 外胚层发育异常/皮肤脆性综合征的组织病理学和超微结构研究
Objective To study clinical and genetic features of hidrotic ectodermal dysplasia ( HED) in Chinese. 目的了解中国人有汗性外胚层发育不良(HED)的临床表现和遗传特点。
Hair and sweat glands in families with hypohidrotic ectodermal dysplasia: Further characterization 少汗性外胚叶发育不良家族中毛发和汗腺的进一步观察
Many ectodermal organs, such as teeth and feathers, all develop from epithelium and mesenchyme. 许多外胚层器官,如牙齿、毛发等均源于上皮组织和间充质组织。