羊膜腔穿刺术诊断为嵌合型15三体综合征，长期随访时15三体细胞系消失。 - Suppr

Disappearance of the trisomy 15 cell line at long-term follow-up in mosaic trisomy 15 at amniocentesis.

作者信息

Chen Chih-Ping

机构信息

Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan; Institute of Clinical and Community Health Nursing, National Yang-Ming University, Taipei, Taiwan; Department of Obstetrics and Gynecology, School of Medicine, National Yang-Ming University, Taipei, Taiwan; Department of Medical Laboratory Science and Biotechnology, Asia University, Taichung, Taiwan.

出版信息

Taiwan J Obstet Gynecol. 2021 Mar;60(2):373. doi: 10.1016/j.tjog.2021.01.021.

DOI:10.1016/j.tjog.2021.01.021

PMID:33678347

Abstract

摘要

相似文献

Disappearance of the trisomy 15 cell line at long-term follow-up in mosaic trisomy 15 at amniocentesis.羊膜腔穿刺术诊断为嵌合型15三体综合征，长期随访时15三体细胞系消失。

Taiwan J Obstet Gynecol. 2021 Mar;60(2):373. doi: 10.1016/j.tjog.2021.01.021.

Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis.在羊膜穿刺术时，培养的和未培养的羊水细胞之间的嵌合性 15 号三体的细胞遗传学差异。

Taiwan J Obstet Gynecol. 2020 Sep;59(5):728-735. doi: 10.1016/j.tjog.2020.07.018.

Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus.羊膜腔穿刺术诊断母体单亲二体 16 相关嵌合性三体 16 合并胎儿的心包积液和宫内生长受限。

Taiwan J Obstet Gynecol. 2021 May;60(3):534-539. doi: 10.1016/j.tjog.2021.03.027.

Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome.羊膜穿刺术诊断低水平嵌合性 17 三体，母源性 17 号染色体单亲二体性，妊娠结局良好。

Taiwan J Obstet Gynecol. 2020 Mar;59(2):301-305. doi: 10.1016/j.tjog.2020.01.021.

Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis in a pregnancy with a favorable outcome.在羊水穿刺检查中，具有良好结局的妊娠中，未培养的羊水细胞与培养的羊水细胞之间的嵌合体 15 三体核型存在差异。

Taiwan J Obstet Gynecol. 2022 Jul;61(4):677-683. doi: 10.1016/j.tjog.2022.05.004.

Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome.在与宫内生长受限和良好结局相关的妊娠中，羊膜穿刺术时发现低水平嵌合体三体 21 合并母体单亲二体 21 的产前诊断。

Taiwan J Obstet Gynecol. 2022 Jan;61(1):146-149. doi: 10.1016/j.tjog.2021.11.025.

Low-level mosaic trisomy 20 without uniparental disomy 20 at amniocentesis in a pregnancy associated with a favorable outcome, cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes and perinatal progressive decrease of the aneuploid cell line.妊娠中期羊膜腔穿刺时发现低水平20号染色体嵌合三体，无20号单亲二体，妊娠结局良好，未培养羊膜细胞与培养羊膜细胞之间存在细胞遗传学差异，且围产期非整倍体细胞系逐渐减少。

Taiwan J Obstet Gynecol. 2023 May;62(3):466-469. doi: 10.1016/j.tjog.2023.03.010.

Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcome.在与宫内生长受限、异常早孕期筛查结果（低 PAPP-A 和低 PlGF）、子痫前期和良好结局相关的妊娠中，羊膜穿刺术时检测到母体单亲二体 9 与低水平嵌合性三体 9 相关。

Taiwan J Obstet Gynecol. 2022 Jan;61(1):141-145. doi: 10.1016/j.tjog.2021.11.024.

Prenatal diagnosis of mosaicism for double aneuploidy of 47,XXY and trisomy 7 (48,XXY,+7) at amniocentesis in a pregnancy with a favorable outcome.羊膜穿刺术诊断出 47,XXY 和 7 三体（48,XXY,+7）双重嵌合体的胚胎嵌合体，此妊娠结局良好。

Taiwan J Obstet Gynecol. 2021 May;60(3):543-548. doi: 10.1016/j.tjog.2021.03.029.

Perinatal cytogenetic discrepancy in a fetus with low-level mosaicism for trisomy 21 and a favorable outcome.胎儿存在低水平三体 21 嵌合体，围产儿细胞遗传学结果不一致，但结局良好。

Taiwan J Obstet Gynecol. 2020 May;59(3):440-442. doi: 10.1016/j.tjog.2020.03.019.

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Disappearance of the trisomy 15 cell line at long-term follow-up in mosaic trisomy 15 at amniocentesis.

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