<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Song S</submitter><funding>Scientific Research Grants of Chongqing Health Center for Women and Children</funding><funding>Joint Scientific Research Grants of Chongqing Health Commission and Science and Technology Bureau</funding><pagination>701</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8522257</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/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).&lt;h4>Case presentation&lt;/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</pubmed_abstract><journal>BMC pregnancy and childbirth</journal><pubmed_title>A very preterm infant born to mother of mirror syndrome secondary to fetomaternal hemorrhage: a case report.</pubmed_title><pmcid>PMC8522257</pmcid><funding_grant_id>2019YJQN01</funding_grant_id><funding_grant_id>2021MSXM116</funding_grant_id><pubmed_authors>Zhou L</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>Jorch G</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Song S</pubmed_authors><pubmed_authors>Zhong X</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors><pubmed_authors>Gong H</pubmed_authors></additional><is_claimable>false</is_claimable><name>A very preterm infant born to mother of mirror syndrome secondary to fetomaternal hemorrhage: a case report.</name><description>&lt;h4>Background&lt;/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).&lt;h4>Case presentation&lt;/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</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-04-04T09:26:55.634Z</modification><creation>2025-04-04T09:26:55.634Z</creation></dates><accession>S-EPMC8522257</accession><cross_references><pubmed>34663239</pubmed><doi>10.1186/s12884-021-04179-5</doi></cross_references></HashMap>