Dr.Hunterthinkscallingitasyndrome,asincomputervisionsyndrome, isa littlemuch. 亨特医生认为称其为电脑视力综合症有点夸张。 www.ebigear.com 5. Hewasdiagnosedwith Asperger'ssyndrome,amildformofautism,sotheythoughthemighthaveproblemsinschool. 他被诊断为雅斯伯格综合症,这是自闭症的一种比较轻的表现症状。因此...
特纳综合征(Turnen`s syndrome)属于先天性发育不全.性染色体异常核型为X染色体单体(XO)或嵌合体(XO/XX或XO/XXX) 两个性染色体中的一个全部或部分丢失所致的性染色体异常常呈现女性表型特纳综合征在活产女性婴儿中的发病率约为/%的X在妊娠早期流产%活产新生儿的X单体来自母亲父系X染色体丢失最常见 婴儿处方患者可在...
The idiopathic Tn-syndrome, formerly called ‘permanent mixed-field polyagglutinability’, is a rare hematological disorder characterized by the expression of the Tn-antigen on all blood cell lineages. The immunodominant epitope of the Tn-antigen is terminal α-N-acetylgalactosamine, O-glycosidically ...
Berger E G.Tn-syndrome. Biochimica et Biophysica Acta . 1999Berger EG. 1999. Tn-syndrome. Biochimica et Biophysica Acta. 1455:255-268.Berger EG. 1999. Tn-syndrome. Biochim. Biophys. Acta 1455:255-268.Berger, E. G., " Tn-syndrome ", Biochim Biophys Acta 1455, (1999) 255-268....
A rare autoimmune disease involving exposure on the surface of erythrocytes, platelets, granulocytes, and lymphocytes of the normally hidden Tn antigen. In patients, both Tn+ and Tn鈥 hematopoietic cells show up and leukemia, thrombocytopenia and nephropathy appear. The Tn membrane glycoprotein is ...
Tn syndrome is a rare autoimmune disease in which subpopulations of blood cells in all lineages carry an incompletely glycosylated membrane glycoprotein, known as the Tn antigen. This truncated antigen has the sugar N-acetyl-galactosamine a-linked toeither a serine or threonine amino-acid residue, ...
特纳综合征特 纳综合征(Turner syndrome,简称 TS)又称先天性卵巢发育不良综合征,是最常见的染色体异常疾病之一,也是人类唯一能生存的单体综合征。特纳综合征是一种仅仅对女性的健康造成影响的疾病。患儿通常少了一条 X 染色体或有异常,影响了女孩正常的骨骼生长和卵巢发育,从而导致了女孩子的生长发育出现异常,同时可能...
对应基因:C1GALT1C1 英文:1、Tn polyagglutination syndrome, somatic(300622, SMu) 中文:1、TN多凝集反应综合征(300622, /) *括号中的数字为OMIM对应编号 括号中的遗传方式:遗传方式指该疾病所呈现的孟德尔遗传方式,分为常染色体显性遗传(AD)、...
The idiopathic Tn-syndrome, formerly called 'permanent mixed-field polyagglutinability', is a rare hematological disorder characterized by the expression of the Tn-antigen on all blood cell lineages. The immunodominant epitope of the Tn-antigen is terminal α- N -acetylgalactosamine, O -glycosidicall...
Tn syndrome is a rare autoimmune disease in which subpopulations of blood cells in all lineages carry an incompletely glycosylated membrane glycoprotein, known as the Tn antigen. This truncated antigen has the sugar N-acetylgalactosamine α-linked to either a serine or threonine amino-acid residue1,...