70 patients ( 63.6%) had positive family history and they showed mostly autosomal dominant inheritance. The rate of consanguinity was 6.9%.

  • 有家族史者70例(63.6%),其中常染色体显性遗传17个家系,近亲结婚者5个家系(6.9%)。
  • 来源:互联网摘选更新时间:2025-01-19 23:32:56

  • 重点词汇
  • positiveadj.积极乐观的;建设性的;拥护的;正面的;明确的;有把握的;阳性的;完全的;大于零的;带正电的;
  • raten.速度,进度;比率;价格,费用;房产税;
  • consanguinityn.血亲,同族,密切关系;同源;
  • showedv. 给…看( show的过去式和过去分词 );表现出;显露出;上演;
  • ofprep. 关于;属于…的;由…制成;
  • 6num. six;
  • wasv. 用来表示某人或某物即主语本身,用来表示某人或某物属于某一群体或有某种性质( be的过去式 );在,存在;不受干扰;
  • andconj. 和,与;而且;于是,然后;因此;
  • hadv.有( have的过去式和过去分词 );(亲属关系中)接受;拿;买到;
  • patientsn.患者( patient的名词复数 );接受治疗者;受动着;承受者;
  • family history家庭史;家庭历;家史;家族来历;
  • 相关例句
1、

The results of genetic analysis in this disease group suggest that hemochromatosis is an autosomal dominant inheritance but not autosomal recessive inheritance disease.

本组病例遗传方式分析结果,不支持常染色体隐性遗传,确定为常染色体显性遗传。

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2、

The hereditary APC-R family was identified, and it appeared to manifest autosomal dominant inheritance. 3.

确定为遗传性APC-R家系,符合常染色体显性遗传规律。

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3、

Conclusions GEFS~+ is autosomal dominant inheritance disease with conspicuous genetic heterogeneity and phenotypic heterogeneity.

结论GEFS+为常染色体显性遗传性疾病,具有显著遗传异质性和表型异质性。

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4、

RESULTS: Of the family investigated, an autosomal dominant inheritance mode with high penetrance and variable expressivity was suggested.

结果:收集的1个3代非综合征型缺牙家系符合常染色体显性遗传,疾病外显率高,但表现度极不一致。

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5、

Conclusion The depressed hypoxia response might have been influenced by genetic factors. The model was in accord with autosomal dominant inheritance.

结论低氧呼吸驱动反应性降低可能受遗传因素的影响,且遗传方式符合常染色体显性遗传;

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6、

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

结论:手掌小鱼际区真实花纹可能属于常染色体显性遗传。

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7、

The results showed that a pat ˉ tern of autosomal dominant inheritance was noticed in all three families.

结果3家系共20例患者,遗传方式均呈常染色体显性遗传;

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8、

Conclusion Genetic factors play a major role in the pathogenesis of familial gallstone disease, characterized by autosomal dominant inheritance.

结论(1)家族性胆囊结石病具有常染色体显性遗传特点,遗传因素是发病的基础。

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9、

Conclusions ( 1) HNPCC is of autosomal dominant inheritance ( AD).

结论(1)该家族呈常染色体显性遗传;

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10、

Two sensory defect congenital nystagmus families accompanying with congenital aniridia showed autosomal dominant inheritance.

2个先天性感觉缺陷性眼球震颤家系皆伴有先天性无虹膜,呈常染色体显性遗传。

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12、

Approximately 2/ 3 of the patients have the family history, and follow the autosomal dominant inheritance pattern.

约2/3的患者有家族病史,表现为常染色体显性遗传,余1/3患者为散发病例。

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13、

The transmission accords with autosomal dominant inheritance.

符合常染色体显性遗传。

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14、

Results The mode of inheritance conforms to autosomal dominant inheritance and polygenic inheritance.

结果遗传方式符合常染色体显性遗传及多基因遗传方式。

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15、

Conclusion: The mode of inheritance of SEDC may be autosomal dominant inheritance.

结论:SEDC遗传方式为常染色体显性遗传。

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16、

The results indicate that psoriasis is of autosomal dominant inheritance and incomplete phenotype.

认为银屑病属于常染色体显性遗传,伴不全表现。

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17、

From all these characteristics autosomal dominant inheritance was unambiguously established.

上述特征完全符合常染色体显性遗传的特点。

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18、

Result: It's autosomal dominant inheritance in this family.

结果:该家族为常染色体显性遗传家系。

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19、

The genetic analysis shows it is autosomal dominant inheritance.

遗传学分析结果显示该家系的遗传方式符合常染色体显性遗传规律。

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20、

It is obviously autosomal dominant inheritance according to the pedigree.

由于第一代病例仅为右眼虹膜缺损,故较支持中胚层迷走发育的理论。

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