...彝首先报道,本征临床并不少见。多囊肾有两种类型,常染色体隐性遗传型(婴儿型)多囊肾(autosomalrecessivepolycystickidneydisease,ARPKD),发病于婴儿期,临床较罕见;常染色体显性遗传型(成年型)多囊肾(autosomaldominantpolycystick...
词条疾病...彝首先报道,本征临床并不少见。多囊肾有两种类型,常染色体隐性遗传型(婴儿型)多囊肾(autosomalrecessivepolycystickidneydisease,ARPKD),发病于婴儿期,临床较罕见;常染色体显性遗传型(成年型)多囊肾(autosomaldominantpolycystick...
词条疾病;泌尿外科;泌尿生殖系先天性畸形;泌尿系先天性畸形;肾畸形...彝首先报道,本征临床并不少见。多囊肾有两种类型,常染色体隐性遗传型(婴儿型)多囊肾(autosomalrecessivepolycystickidneydisease,ARPKD),发病于婴儿期,临床较罕见;常染色体显性遗传型(成年型)多囊肾(autosomaldominantpolycystick...
词条疾病;泌尿外科;泌尿生殖系先天性畸形;泌尿系先天性畸形;肾畸形...彝首先报道,本征临床并不少见。多囊肾有两种类型,常染色体隐性遗传型(婴儿型)多囊肾(autosomalrecessivepolycystickidneydisease,ARPKD),发病于婴儿期,临床较罕见;常染色体显性遗传型(成年型)多囊肾(autosomaldominantpolycystick...
词条疾病;泌尿外科;泌尿生殖系先天性畸形;泌尿系先天性畸形;肾畸形...彝首先报道,本征临床并不少见。多囊肾有两种类型,常染色体隐性遗传型(婴儿型)多囊肾(autosomalrecessivepolycystickidneydisease,ARPKD),发病于婴儿期,临床较罕见;常染色体显性遗传型(成年型)多囊肾(autosomaldominantpolycystick...
词条疾病;泌尿外科;泌尿生殖系先天性畸形;泌尿系先天性畸形;肾畸形...彝首先报道,本征临床并不少见。多囊肾有两种类型,常染色体隐性遗传型(婴儿型)多囊肾(autosomalrecessivepolycystickidneydisease,ARPKD),发病于婴儿期,临床较罕见;常染色体显性遗传型(成年型)多囊肾(autosomaldominantpolycystick...
词条疾病;泌尿外科;泌尿生殖系先天性畸形;泌尿系先天性畸形;肾畸形...彝首先报道,本征临床并不少见。多囊肾有两种类型,常染色体隐性遗传型(婴儿型)多囊肾(autosomalrecessivepolycystickidneydisease,ARPKD),发病于婴儿期,临床较罕见;常染色体显性遗传型(成年型)多囊肾(autosomaldominantpolycystick...
词条疾病;泌尿外科;泌尿生殖系先天性畸形;泌尿系先天性畸形;肾畸形...彝首先报道,本征临床并不少见。多囊肾有两种类型,常染色体隐性遗传型(婴儿型)多囊肾(autosomalrecessivepolycystickidneydisease,ARPKD),发病于婴儿期,临床较罕见;常染色体显性遗传型(成年型)多囊肾(autosomaldominantpolycystick...
词条疾病;泌尿外科;泌尿生殖系先天性畸形;泌尿系先天性畸形;肾畸形...血清前体APP的基因与家族性早老性痴呆症基因均位于21号染色体的长臂上,但两者并不联锁。关于β-蛋白与早老性痴呆症的神经功能紊乱和损伤之间的关系,还未取得一致意见。但APP突变确可引起早老性痴呆症,而Down综合征(21号...
词条疾病;营养科...三)肝豆状核变性(hepatolenticulardegeneration) 是一种常染色体隐性遗传的铜代谢障碍的家族性疾病。常侵犯儿或青年人,临床上表现进行性加剧的肢体震颤、肌强直、构音困难、精神改变、肝硬化及角膜色素环等症状。尿铜量...
参考资料求医问药;疾病大全;头部