{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,26]],"date-time":"2025-11-26T08:30:01Z","timestamp":1764145801762,"version":"3.46.0"},"reference-count":9,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,11,26]]},"DOI":"10.7759\/cureus.97824","type":"journal-article","created":{"date-parts":[[2025,11,26]],"date-time":"2025-11-26T08:24:56Z","timestamp":1764145496000},"source":"Crossref","is-referenced-by-count":0,"title":["A Male Child With Combined Glucose-6-Phosphate Dehydrogenase Deficiency and Hereditary Elliptocytosis: The First Case Reported From Saudi Arabia"],"prefix":"10.7759","author":[{"given":"Badriah G","family":"Alasmari","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fahad F","family":"Al Munajjim","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shady","family":"Wafa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ayman","family":"Abualama","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lina","family":"Elzubair","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1016\/j.bcmd.2008.12.005","article-title":"The global prevalence of glucose-6-phosphate dehydrogenase deficiency: a systematic review and meta-analysis","volume":"42","author":"Nkhoma ET","year":"2009","unstructured":"Nkhoma ET, Poole C, Vannappagari V, Hall SA, Beutler E. The global prevalence of glucose-6-phosphate dehydrogenase deficiency: a systematic review and meta-analysis. Blood Cells Mol Dis. 2009, 42:267-78. 10.1016\/j.bcmd.2008.12.005","journal-title":"Blood Cells Mol Dis"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1182\/blood.2019000944","article-title":"Glucose-6-phosphate dehydrogenase deficiency","volume":"136","author":"Luzzatto L","year":"2020","unstructured":"Luzzatto L, Ally M, Notaro R. Glucose-6-phosphate dehydrogenase deficiency. Blood. 2020, 136:1225-40. 10.1182\/blood.2019000944","journal-title":"Blood"},{"key":"ref3","article-title":"Hereditary elliptocytosis","author":"Jha SK","year":"2025","unstructured":"Jha SK, Vaqar S. Hereditary elliptocytosis. StatPearls. StatPearls Publishing, Treasure Island; 2025."},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1182\/asheducation-2005.1.13","article-title":"Red cell membrane disorders","author":"Gallagher PG","year":"2005","unstructured":"Gallagher PG. Red cell membrane disorders. Hematology Am Soc Hematol Educ Program. 2005, 13-8. 10.1182\/asheducation-2005.1.13","journal-title":"Hematology Am Soc Hematol Educ Program"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.3346\/jkms.2024.39.e162","article-title":"Current status of molecular diagnosis of hereditary hemolytic anemia in Korea","volume":"39","author":"Chueh HW","year":"2024","unstructured":"Chueh HW, Shim YJ, Jung HL, Kim N, Hwang SM, Kim M, Choi HS. Current status of molecular diagnosis of hereditary hemolytic anemia in Korea. J Korean Med Sci. 2024, 39:e162. 10.3346\/jkms.2024.39.e162","journal-title":"J Korean Med Sci"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.5045\/br.2017.52.2.84","article-title":"Diagnostic approaches for inherited hemolytic anemia in the genetic era","volume":"52","author":"Kim Y","year":"2017","unstructured":"Kim Y, Park J, Kim M. Diagnostic approaches for inherited hemolytic anemia in the genetic era. Blood Res. 2017, 52:84-94. 10.5045\/br.2017.52.2.84","journal-title":"Blood Res"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.4065\/76.3.285","article-title":"Hereditary red blood cell disorders in middle eastern patients","volume":"76","author":"Steensma DP","year":"2001","unstructured":"Steensma DP, Hoyer JD, Fairbanks VF. Hereditary red blood cell disorders in middle eastern patients. Mayo Clin Proc. 2001, 76:285-93. 10.4065\/76.3.285","journal-title":"Mayo Clin Proc"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1353\/hub.2005.0004","article-title":"Hemoglobinopathies, G6PD deficiency, and hereditary elliptocytosis in Bahrain","volume":"76","author":"Dash S","year":"2004","unstructured":"Dash S. Hemoglobinopathies, G6PD deficiency, and hereditary elliptocytosis in Bahrain. Hum Biol. 2004, 76:779-83. 10.1353\/hub.2005.0004","journal-title":"Hum Biol"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2141.1993.tb04679.x","article-title":"Blood film features of sickle cell-haemoglobin C disease","volume":"83","author":"Bain BJ","year":"1993","unstructured":"Bain BJ. Blood film features of sickle cell-haemoglobin C disease. Br J Haematol. 1993, 83:516-8. 10.1111\/j.1365-2141.1993.tb04679.x","journal-title":"Br J Haematol"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/437100-a-male-child-with-combined-glucose-6-phosphate-dehydrogenase-deficiency-and-hereditary-elliptocytosis-the-first-case-reported-from-saudi-arabia","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,11,26]],"date-time":"2025-11-26T08:24:58Z","timestamp":1764145498000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/437100-a-male-child-with-combined-glucose-6-phosphate-dehydrogenase-deficiency-and-hereditary-elliptocytosis-the-first-case-reported-from-saudi-arabia"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,11,26]]},"references-count":9,"URL":"https:\/\/doi.org\/10.7759\/cureus.97824","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2025,11,26]]}}}