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胎儿脑白质营养不良伴免疫缺陷、鱼鳞病和毛发稀疏症的产前诊断

Prenatal diagnosis of PIBIDS.

作者信息

Savary J B, Vasseur F, Vinatier D, Manouvrier S, Thomas P, Deminatti M M

机构信息

Laboratoire de Génétique Humaine, Pathologie Foetale (Pr. Deminatti), Faculté de Médecine, Lille, France.

出版信息

Prenat Diagn. 1991 Nov;11(11):859-66. doi: 10.1002/pd.1970111107.

Abstract

In a well-documented PIBIDS family, two investigations of DNA excision repair showed a severe defect in lymphocytes from the index case (residual repair activities were 10.6-12.1 per cent). The values for the mother, father, and sister were within the normal range when compared with a healthy control. In the pregnant mother, a prenatal diagnosis of PIBIDS was made by measuring UV-induced unscheduled DNA synthesis in cultivated amniotic fluid cells. Results ranged between 12.5 and 26.1 per cent depending on the UV doses applied and were consistent with an affected fetus. The parents opted for a termination of pregnancy. Following a therapeutic abortion, fetal skin fibroblasts were tested and showed a severe DNA excision-repair defect of 9.2-13.5 per cent of residual activity.

摘要

在一个有充分文献记载的PIBIDS家族中,两项DNA切除修复研究显示,先证者淋巴细胞存在严重缺陷(残余修复活性为10.6%-12.1%)。与健康对照相比,母亲、父亲和姐姐的值在正常范围内。在怀孕母亲中,通过测量培养羊水细胞中紫外线诱导的非预定DNA合成对PIBIDS进行产前诊断。根据所施加的紫外线剂量,结果在12.5%至26.1%之间,与受影响的胎儿一致。父母选择终止妊娠。治疗性流产后,对胎儿皮肤成纤维细胞进行检测,显示残余活性严重的DNA切除修复缺陷为9.2%-13.5%。

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