{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,15]],"date-time":"2025-11-15T06:02:58Z","timestamp":1763186578940,"version":"3.45.0"},"reference-count":17,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2025,9,25]],"date-time":"2025-09-25T00:00:00Z","timestamp":1758758400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Transfusion"],"published-print":{"date-parts":[[2025,11]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      Deficiency of Rh antigens affects the red blood cell (RBC) membrane integrity, thus reducing erythrocyte survival, clinically manifesting as chronic hemolytic anemia. Various mutations cause such Rh\n                      <jats:sub>null\/mod<\/jats:sub>\n                      phenotypes. Parvovirus B19 infection causes transient red cell aplasia, leading to potentially severe anemia in patients with chronic hemolytic disorders.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Study Design and Methods<\/jats:title>\n                    <jats:p>A patient with known, etiologically unclear mild chronic anemia presented with a syncopal event. Clinical and laboratory work\u2010up, including targeted genetic analyses of RBC genes, was performed.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The patient was severely anemic with moderate signs of hemolysis and evidence of impaired erythropoiesis. Immunohematological work\u2010up identified a lack of Rh antigen expression. A homozygous\n                      <jats:italic>c.1034G&gt;A<\/jats:italic>\n                      missense mutation in\n                      <jats:italic>RHAG<\/jats:italic>\n                      adequately explains this finding, as well as the chronic hemolysis. Parvovirus B19 was identified as causal for the acute aplastic crisis.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Discussion<\/jats:title>\n                    <jats:p>\n                      This is the first clinical report of parvovirus B19\u2010related red cell aplasia in a patient with the\n                      <jats:italic>RHAG*01M.15<\/jats:italic>\n                      phenotype.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/trf.18378","type":"journal-article","created":{"date-parts":[[2025,9,26]],"date-time":"2025-09-26T05:21:27Z","timestamp":1758864087000},"page":"2203-2206","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Transient severe anemia triggered by parvovirus\n                    <scp>B19<\/scp>\n                    infection in a patient with homozygous\n                    <scp>RhAG<\/scp>\n                    deficiency"],"prefix":"10.1111","volume":"65","author":[{"given":"Anna","family":"Hausdorf","sequence":"first","affiliation":[{"name":"German Red Cross Blood Service Baden\u2010W\u00fcrttemberg\u2010Hesse Institute Frankfurt  Frankfurt am Main Germany"},{"name":"Department of Hematology and Oncology Municipal Hospital Frankfurt\u2010H\u00f6chst  Frankfurt am Main Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hans\u2010G\u00fcnter","family":"Derigs","sequence":"additional","affiliation":[{"name":"Department of Hematology and Oncology Municipal Hospital Frankfurt\u2010H\u00f6chst  Frankfurt am Main Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0088-2675","authenticated-orcid":false,"given":"Halvard","family":"Bonig","sequence":"additional","affiliation":[{"name":"German Red Cross Blood Service Baden\u2010W\u00fcrttemberg\u2010Hesse Institute Frankfurt  Frankfurt am Main Germany"},{"name":"Goethe University Medical School Institute for Transfusion Medicine and Immunohematology  Frankfurt am Main Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Erika","family":"Fleck","sequence":"additional","affiliation":[{"name":"German Red Cross Blood Service Baden\u2010W\u00fcrttemberg\u2010Hesse Institute Frankfurt  Frankfurt am Main Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0038-385X","authenticated-orcid":false,"given":"Susanne","family":"Braeuninger","sequence":"additional","affiliation":[{"name":"German Red Cross Blood Service Baden\u2010W\u00fcrttemberg\u2010Hesse Institute Frankfurt  Frankfurt am Main Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2025,9,25]]},"reference":[{"volume-title":"Guideline on haemoglobin cutoffs to define anaemia in individuals and populations","year":"2024","author":"World Health Organization","key":"e_1_2_4_2_1"},{"key":"e_1_2_4_3_1","doi-asserted-by":"publisher","DOI":"10.1002\/jcla.1039"},{"key":"e_1_2_4_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(61)92183-3"},{"key":"e_1_2_4_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0037-1963(00)90040-4"},{"issue":"6","key":"e_1_2_4_6_1","first-page":"623","article-title":"An unlinked modifier of Rh blood groups: effects when heterozygous and when homozygous","volume":"24","author":"Chown B","year":"1972","journal-title":"Am J Hum Genet"},{"key":"e_1_2_4_7_1","unstructured":"International Society of Blood Transfusion (ISBT).(ISBT 030) RHAG blood group alleles v6.4 31\u2010JUL\u20102023. 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