{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Song S"],"funding":["Scientific Research Grants of Chongqing Health Center for Women and Children","Joint Scientific Research Grants of Chongqing Health Commission and Science and Technology Bureau"],"pagination":["701"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8522257"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["21(1)"],"pubmed_abstract":["<h4>Background</h4>Mirror syndrome (MS) is defined as maternal edema with fetal hydrops and placental edema with different etiologies, such as rhesus isoimmunization and twin-twin transfusion syndrome. Herein, we showcased a unique MS case secondary to fetomaternal hemorrhage (FMH).<h4>Case presentation</h4>A 32-year-old gravida 2 para 0 woman diagnosed with fetal hydrops was admitted to our hospital. Maternal laboratory tests revealed anemia, slightly increased creatinine and uric acid levels, hypoproteinemia, and significantly increased alpha-fetoprotein and hemoglobin-F levels. Therefore, FMH was diagnosed initially. Two days after admission, the woman had unexpectedly progressive anasarca and started to feel chest distress, palpitations, lethargy, and oliguria, and MS was suspected. An"],"journal":["BMC pregnancy and childbirth"],"pubmed_title":["A very preterm infant born to mother of mirror syndrome secondary to fetomaternal hemorrhage: a case report."],"pmcid":["PMC8522257"],"funding_grant_id":["2019YJQN01","2021MSXM116"],"pubmed_authors":["Zhou L","Zhu Y","Jorch G","Zhang X","Chen W","Song S","Zhong X","Wang X","Wu Y","Gong H"],"additional_accession":[]},"is_claimable":false,"name":"A very preterm infant born to mother of mirror syndrome secondary to fetomaternal hemorrhage: a case report.","description":"<h4>Background</h4>Mirror syndrome (MS) is defined as maternal edema with fetal hydrops and placental edema with different etiologies, such as rhesus isoimmunization and twin-twin transfusion syndrome. Herein, we showcased a unique MS case secondary to fetomaternal hemorrhage (FMH).<h4>Case presentation</h4>A 32-year-old gravida 2 para 0 woman diagnosed with fetal hydrops was admitted to our hospital. Maternal laboratory tests revealed anemia, slightly increased creatinine and uric acid levels, hypoproteinemia, and significantly increased alpha-fetoprotein and hemoglobin-F levels. Therefore, FMH was diagnosed initially. Two days after admission, the woman had unexpectedly progressive anasarca and started to feel chest distress, palpitations, lethargy, and oliguria, and MS was suspected. An","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 Oct","modification":"2025-04-04T09:26:55.634Z","creation":"2025-04-04T09:26:55.634Z"},"accession":"S-EPMC8522257","cross_references":{"pubmed":["34663239"],"doi":["10.1186/s12884-021-04179-5"]}}