儿科常规
...生育次数,有无流产、早产、多胎或分娩过新生儿溶血症婴儿等。(2)兄弟姐妹情况兄弟姐妹各几人,按顺序注明各人年龄及健康情况;如死亡,应叙述死因。对家庭成员均须询问有无肝炎、结核、变态反应性疾病或其他遗传性疾...
经胸部径路气管食管瘘修补及食管一期吻合术
...多,喂食后可立即发生呕吐、呛咳并发绀。有远端瘘管的婴儿,气体可经瘘管进入胃及消化道,使腹部膨胀增大。因唾液流入呼吸道及胃液反流经瘘管进入呼吸道,加之膈上升压迫肺脏,出现明显呼吸困难。当发现这些征象时应...
胸外科手术;食管手术;食管先天性异常的手术治疗;先天性食管闭锁及食管气管瘘的手术治疗;气管食管瘘修补术;手术多囊肾
...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(autosomaldominantpolycystickidneydisease,ADPKD),常...
疾病多囊病
...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(autosomaldominantpolycystickidneydisease,ADPKD),常...
疾病;泌尿外科;泌尿生殖系先天性畸形;泌尿系先天性畸形;肾畸形囊胞肾
...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(autosomaldominantpolycystickidneydisease,ADPKD),常...
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Perlmann综合征
...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(autosomaldominantpolycystickidneydisease,ADPKD),常...
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Potter(Ⅰ)综合征
...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(autosomaldominantpolycystickidneydisease,ADPKD),常...
疾病;泌尿外科;泌尿生殖系先天性畸形;泌尿系先天性畸形;肾畸形肾脏良性多房性囊瘤
...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(autosomaldominantpolycystickidneydisease,ADPKD),常...
疾病;泌尿外科;泌尿生殖系先天性畸形;泌尿系先天性畸形;肾畸形双侧肾发育不全综合征
...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(autosomaldominantpolycystickidneydisease,ADPKD),常...
疾病;泌尿外科;泌尿生殖系先天性畸形;泌尿系先天性畸形;肾畸形先天性先天性肾囊肿瘤病
...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(autosomaldominantpolycystickidneydisease,ADPKD),常...
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