{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,21]],"date-time":"2025-09-21T17:01:41Z","timestamp":1758474101806,"version":"3.40.4"},"reference-count":12,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Reports"],"accepted":{"date-parts":[[2016,12,23]]},"abstract":"<jats:p>A 33-week gestation boy with Mediterranean glucose-6-phosphate dehydrogenase (G6PD) and a glutathione<jats:italic>S<\/jats:italic>-transferase Mu 1 null mutations (GSTM1*0\/*0) developed prolonged indirect hyperbilirubinemia (PIH). He had no laboratory evidence of haemolysis or infection, and no exposure to oxidising agents. He has two full-term older brothers who have no history of neonatal hyperbilirubinemia. One brother, who was exclusively breast fed, has only Mediterranean G6PD and the other has only GSTM1*0\/*0. The three boys have no mutation in the uridine diphosphate glucuronosyltransferase 1A1 gene. This suggests that a combination of all or any two of prematurity, G6PD deficiency and GSTM1*0\/*0 is a possible risk factor for PIH. However, this remains to be confirmed.<\/jats:p>","DOI":"10.1136\/bcr-2016-218404","type":"journal-article","created":{"date-parts":[[2017,1,9]],"date-time":"2017-01-09T15:40:14Z","timestamp":1483976414000},"page":"bcr2016218404","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":1,"title":["Prolonged indirect hyperbilirubinemia in a moderately preterm boy with Mediterranean glucose-6-phosphate dehydrogenase and glutathione<i>S<\/i>-transferase Mu 1 null mutations"],"prefix":"10.1136","volume":"2017","author":[{"given":"Sameer Yaseen","family":"Al-Abdi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2017,1,9]]},"reference":[{"key":"2025042702212588000_2017.jan09_1.bcr2016218404.1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1442-200X.2010.03170.x"},{"key":"2025042702212588000_2017.jan09_1.bcr2016218404.2","doi-asserted-by":"publisher","DOI":"10.1542\/peds.2013-4299"},{"key":"2025042702212588000_2017.jan09_1.bcr2016218404.3","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1038\/sj.jp.7211448","article-title":"Glucose-6-phosphate dehydrogenase deficiency in triplets of African-American descent","volume":"26","author":"Turbendian","year":"2006","journal-title":"J Perinatol"},{"key":"2025042702212588000_2017.jan09_1.bcr2016218404.4","doi-asserted-by":"crossref","first-page":"475","DOI":"10.1002\/pbc.22046","article-title":"A prolonged neonatal jaundice associated with a rare G6PD mutation","volume":"53","author":"Minucci","year":"2009","journal-title":"Pediatric blood Cancer"},{"key":"2025042702212588000_2017.jan09_1.bcr2016218404.5","doi-asserted-by":"crossref","unstructured":"Al-Abdi SY . 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