成骨不全的分子机制成骨不全(osteogenesis imperfecta,OI),又称脆骨病(brittle bone disease),是一种由于间充质组织发育不全,胶原形成障碍而造成的罕见遗传性疾病[1,2].多数为常染色体显性遗传,少数为常染色体隐性遗传.
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成骨不全( osteogenesis imperfecta , OI )又称脆骨症( brittle bone disease ),是一种常染色体遗传的先天性疾病,由遗传性中胚层发育障碍造成骨骼脆性增加及胶原蛋白代谢紊乱为特征的结缔组织异常性疾病。
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...混乱,在报告中曾用过的名称有:鸡苍白综合症(Pale bird Syndrome),直升飞机病(Helicopter disease),骨脆病(Brittle bone disease),传染性前胃炎(Proventriculitis),骨质疏松病(Osteoporosis),吸收不良综合症(Malabsorption syndrome),以及传染性矮小综合症(Inf...
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N → the nontechnical name for osteogenesis imperfecta
Mostly, he sits in a wheelchair, crippled by brittle bone disease.
由于脆骨病致残,他大多数情况下坐在轮椅上。
A third had developed lung disease, dementia, diabetes, heart disease, high blood pressure, brittle bone disease and Parkinson's or had a stroke before the age of 85 and lived with the effects.
第三个课题是研究85岁前已经患有肺病、痴呆、糖尿病、心脏病、高血压、脆骨病和帕金森或患中风的老人以及带病生活的结果。
Osteoporosis is a bone-wasting disease that makes your bones brittle and more prone to breaks.
骨骼疏松症是一种使你的骨骼脆弱和甚至破坏的骨骼损耗疾病。
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