{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T11:45:18Z","timestamp":1790163918823,"version":"4.1.0"},"reference-count":35,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2025,4,25]],"date-time":"2025-04-25T00:00:00Z","timestamp":1745539200000},"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":["Br J Haematol"],"published-print":{"date-parts":[[2025,6]]},"abstract":"<jats:title>Summary<\/jats:title>\n                  <jats:p>Fetal\u2013neonatal alloimmune thrombocytopenia (FNAIT) results from parental platelet antigen incompatibility, with human platelet antigen (HPA)\u20101a the most common. Human leukocyte antigen (HLA)\u2010DRB3*01:01 is strongly associated with the development of high titre anti\u2010HPA\u20101a antibodies and B8DR3 with autoimmunity. Investigation of FNAIT has focused on fetal\u2013neonatal haemorrhagic, placental and neurodevelopmental effects but has not included mothers. Symptomatic complaints pointing to autoimmunity from FNAIT\u2010affected mothers along with HLA\u00a0overlap for FNAIT\/autoimmunity (HLA\u2010DRB3*01:01, B8DR3) prompted exploration of autoimmune disorders. A de\u2010identified survey sent to NAITbabies mothers included medical review of systems with additional questions on autoimmunity. The frequency of autoimmunity in FNAIT mothers plus its fetal impact was explored. 125\/232 (54%) of FNAIT mothers reported psychological problems &gt;6\u2009weeks, with 90% reporting \u2018anxiety\u2019 and &gt;50% reporting each of stress, depression and sleep disturbances. Symptoms were more frequent in mothers whose child did not survive their intracranial hemorrhage (ICH)\u00a0and those with multiple FNAIT\u2010affected children. The next most common medical symptoms were gastrointestinal and musculoskeletal with 30% frequency. Autoimmunity was mildly increased in mothers with FNAIT, for example, thyroiditis and three other B8DR3\u2010related diseases. Autoimmunity did not worsen neonatal ICH incidence or birthweight. By exploring affected mothers, this study expands the spectrum of diseases associated with FNAIT to include maternal autoimmunity and especially psychological symptoms.<\/jats:p>","DOI":"10.1111\/bjh.20112","type":"journal-article","created":{"date-parts":[[2025,4,25]],"date-time":"2025-04-25T04:03:58Z","timestamp":1745553838000},"page":"1754-1763","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":6,"title":["Fetal\u2013neonatal alloimmune thrombocytopenia: Mothers are affected too"],"prefix":"10.1111","volume":"206","author":[{"ORCID":"https:\/\/orcid.org\/0009-0007-7157-1213","authenticated-orcid":false,"given":"Eleanore A.","family":"McFarland","sequence":"first","affiliation":[{"name":"Weill Cornell Medicine  New York New York USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Emilie L.","family":"Vander Haar","sequence":"additional","affiliation":[{"name":"Weill Cornell Medicine  New York New York 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