Noninvasive prenatal testing suggesting an abnormality in chromosome 15 confirmed to be a case of Prader–Willi syndrome caused by trisomy rescue in the neonatal period-Reference-Cited by-同舟云学术

Noninvasive prenatal testing suggesting an abnormality in chromosome 15 confirmed to be a case of Prader–Willi syndrome caused by trisomy rescue in the neonatal period

Published:2022-03-23 Issue:8 Volume:48 Page:2214-2218
ISSN:1341-8076
Container-title:Journal of Obstetrics and Gynaecology Research
language:en
Short-container-title:J of Obstet and Gynaecol

Author:

Okuda Tomohiro¹^ORCID,Moroto Masaharu²,Yamamoto Toshiyuki³

Affiliation:

1. Department of Obstetrics and Gynecology Fukuchiyama City Hospital Fukuchiyama City Kyoto Japan

2. Department of Pediatrics Fukuchiyama City Hospital Fukuchiyama City Kyoto Japan

3. Institute of Medical Genetics Tokyo Women's Medical University Tokyo Japan

Publisher

Wiley

Subject

Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jog.15236

Reference14 articles.

1. Prader-Willi syndrome

2. Maternal age effect on the development of Prader–Willi syndrome resulting from upd(15)mat through meiosis 1 errors

3. Prader–Willi syndrome

4. Possibility of early diagnosis in a fetus affected by Prader‐Willi syndrome with maternal hetero‐UPD15: a lesson to be learned;Dong Y;Mol Med Rep,2019

5. Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancy

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1. Low-level mosaic trisomy 15 at amniocentesis without uniparental disomy 15 in a pregnancy associated with cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes, a favorable fetal outcome and perinatal decrease of the aneuploid cell line;Taiwanese Journal of Obstetrics and Gynecology;2023-03