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- atrophia bulborum hereditaria 诺里(氏)病:一种X-链锁遗传病, 包括双侧视网膜异常而引起失明, 继之可发生智力迟钝和耳聋
- atrophia bulborum bereditaria 胎儿虹膜炎综合征, 遗传性眼球萎缩
- To introduce the mechanism of atrophia diseases briefly. 分析痿病毒损络脉的机制。
- Objective To analyse the mutation of ADAR gene in a pedigree with dyschromatosis symmetrical hereditaria. 目的探讨遗传性对称性色素异常症(DSH)一家系ADAR基因突变情况。
- Objective To study the diagnosis and surgical operation in the treatment of temporal lobe epilepsy with hippocampal atrophia. 目的对仅有海马萎缩(硬化)的颞叶癫痫的诊断和手术治疗作一探讨。
- Results In the 42eyes,Visual acuity of 35 eyes were improved in varied degree. 5 eyes was atrophia, 2 eyes inflammation was not controled. 结果 42例患者35眼视力有不同程度提高，5眼眼球萎缩，2眼炎症未控制行眼球摘除。
- Gastric pit,especially its type D and type E,as featured pathological changes,suggested the genesis of stomach membrane atrophia. 胃小凹的特征性改变,尤其是D型、E型胃小凹的出现极大地提示胃黏膜萎缩的形成。
- telangiectasia hereditaria haemorrhagica 遗传性出血性毛细血管扩张
- telangiectasis hereditaria hemorrhagica 出血性遗传性毛细血管扩张
- dyschromatosis symmetrical hereditaria 遗传性对称性色素异常症
- epidermolysis bullosa hereditaria 遗传性大疱性表皮松解
- Epidermolysis bullosa hereditaria letalis 致命性大疱性表皮松解
- atrophia cerebri senilis simplex 单纯性老年性脑萎缩
- atrophia choriideae circumpapillaris 视乳头周围脉络膜萎缩
- epidermolysis bullosa hereditaria lethalis (拉)先天性大疱性致死性表皮松解
- acrodystrophia universalis hereditaria 遗传性普遍性肢营养不良
- atrophia chorioideae circumpapillaris 视乳头周围脉络膜萎缩
- atrophia chorioiretinalis disseminata 播散性脉膜视网膜萎缩
- porphyria cutanea tarda hereditaria 遗传性原粪卟啉症
- cristallinea cornea hereditaria degeneratio 遗传性角膜结晶状变性
