{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,9,6]],"date-time":"2024-09-06T12:52:26Z","timestamp":1725627146671},"reference-count":13,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2021,7,1]]},"DOI":"10.7759\/cureus.16081","type":"journal-article","created":{"date-parts":[[2021,7,1]],"date-time":"2021-07-01T08:53:46Z","timestamp":1625129626000},"source":"Crossref","is-referenced-by-count":1,"title":["Congenital Methemoglobinemia and Unstable Hemoglobin Variant in a Child With Cyanosis"],"prefix":"10.7759","author":[{"given":"Mohammed","family":"Alsabri","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kusum","family":"Viswanathan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anthony","family":"Elias","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mario","family":"Peichev","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","article-title":"A case of congenital cyanosis without an apparent cause","volume":"4","author":"Francois","year":"1845","unstructured":"Francois. A case of congenital cyanosis without an apparent cause. Bull Acad Roy Med Belg. 1845, 4:698.","journal-title":"Bull Acad Roy Med Belg"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1002\/ajh.2830420103","article-title":"Historical note: methemoglobinemia--long ago and far away","volume":"42","author":"Gibson QH","year":"1993","unstructured":"Gibson QH. Historical note: methemoglobinemia--long ago and far away. Am J Hematol. 1993, 42:3-6. 10.1002\/ajh.2830420103","journal-title":"Am J Hematol"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1016\/S0021-9258(19)88718-5","article-title":"Enzymatic instability of NADH-cytochrome b5 reductase as a cause of hereditary methemoglobinemia type I (red cell type)","volume":"267","author":"Shirabe K","year":"1992","unstructured":"Shirabe K, Yubisui T, Borgese N, Tang CY, Hultquist DE, Takeshita M. Enzymatic instability of NADH-cytochrome b5 reductase as a cause of hereditary methemoglobinemia type I (red cell type). J Biol Chem. 1992, 267:20416. 10.1016\/S0021-9258(19)88718-5","journal-title":"J Biol Chem"},{"key":"ref4","article-title":"Methemoglobinemia: a systematic review of the pathophysiology, detection, and treatment","volume":"83","author":"Ashurst J","year":"2011","unstructured":"Ashurst J, Wasson M. Methemoglobinemia: a systematic review of the pathophysiology, detection, and treatment. Del Med J. 2011, 83:203-208.","journal-title":"Del Med J"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1016\/0006-3002(59)90324-5","article-title":"The enzymic defect of hereditary methemoglobinemia: diaphorase","volume":"34","author":"Scott EM","year":"1959","unstructured":"Scott EM, Griffith IV. The enzymic defect of hereditary methemoglobinemia: diaphorase. Biochim Biophys Acta. 1959, 34:584-586. 10.1016\/0006-3002(59)90324-5","journal-title":"Biochim Biophys Acta"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2141.1981.tb02803.x","article-title":"Methaemoglobinaemia resulting from heterozygosity for two NADH-methaemoglobin reductase variants: characterization as NADH-ferricyanide reductase","volume":"47","author":"Board PG","year":"1981","unstructured":"Board PG, Pidcock ME. Methaemoglobinaemia resulting from heterozygosity for two NADH-methaemoglobin reductase variants: characterization as NADH-ferricyanide reductase. Br J Haematol. 1981, 47:361-370. 10.1111\/j.1365-2141.1981.tb02803.x","journal-title":"Br J Haematol"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1111\/j.1600-0609.1978.tb02472.x","article-title":"Heterogeneity of hereditary methaemoglobinaemia: a study of 4 Cuban families with NADH-Methaemoglobin reductase deficiency including a new variant (Santiago de Cuba variant)","volume":"20","author":"Gonz\u00e1lez R","year":"1978","unstructured":"Gonz\u00e1lez R, Estrada M, Wade M, et al.. Heterogeneity of hereditary methaemoglobinaemia: a study of 4 Cuban families with NADH-Methaemoglobin reductase deficiency including a new variant (Santiago de Cuba variant). Scand J Haematol. 1978, 20:385-393. 10.1111\/j.1600-0609.1978.tb02472.x","journal-title":"Scand J Haematol"},{"key":"ref8","article-title":"Cytochrome b5 reductase deficiency and enzymopenic hereditary methemoglobinemia","author":"Jaffe E","year":"1995","unstructured":"Jaffe E, Hultquist D. Cytochrome b5 reductase deficiency and enzymopenic hereditary methemoglobinemia. In: The Metabolic and Molecular Bases of Inherited Disease. Scriver C, Beaudet A, Sly W, Valle D (ed): McGraw Hill, New York; 1995. 3:3399."},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1021\/bi00420a007","article-title":"Hemoglobin Brockton [beta 138 (H16) Ala----Pro]: an unstable variant near the C-terminus of the beta-subunits with normal oxygen-binding properties","volume":"27","author":"Moo-Penn WF","year":"1988","unstructured":"Moo-Penn WF, Jue DL, Johnson MH, et al.. Hemoglobin Brockton [beta 138 (H16) Ala----Pro]: an unstable variant near the C-terminus of the beta-subunits with normal oxygen-binding properties. Biochemistry. 1988, 27:7614-7619. 10.1021\/bi00420a007","journal-title":"Biochemistry"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.83.16.6137","article-title":"Co-clustering of denatured hemoglobin with band 3: its role in binding of autoantibodies against band 3 to abnormal and aged erythrocytes","volume":"83","author":"Schl\u00fcter K","year":"1986","unstructured":"Schl\u00fcter K, Drenckhahn D. Co-clustering of denatured hemoglobin with band 3: its role in binding of autoantibodies against band 3 to abnormal and aged erythrocytes. Proc Natl Acad Sci U S A. 1986, 83:6137-6141. 10.1073\/pnas.83.16.6137","journal-title":"Proc Natl Acad Sci U S A"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1136\/bcr-2018-228470","article-title":"Congenital methaemoglobinaemia diagnosed in an adolescent boy","volume":"12","author":"Paul A","year":"2019","unstructured":"Paul A, Chacko ST. Congenital methaemoglobinaemia diagnosed in an adolescent boy. BMJ Case Rep. 2019, 12:228470. 10.1136\/bcr-2018-228470","journal-title":"BMJ Case Rep"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2141.2008.07017.x","article-title":"Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency","volume":"141","author":"Percy MJ","year":"2008","unstructured":"Percy MJ, Lappin TR. Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency. Br J Haematol. 2008, 141:298-308. 10.1111\/j.1365-2141.2008.07017.x","journal-title":"Br J Haematol"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.1542\/peds.2018-2814","article-title":"Congenital methemoglobinemia identified by pulse oximetry screening","volume":"143","author":"Ward J","year":"2019","unstructured":"Ward J, Motwani J, Baker N, Nash M, Ewer AK, Toldi G. Congenital methemoglobinemia identified by pulse oximetry screening. Pediatrics. 2019, 143:e20182814. 10.1542\/peds.2018-2814","journal-title":"Pediatrics"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/63241-congenital-methemoglobinemia-and-unstable-hemoglobin-variant-in-a-child-with-cyanosis","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T19:31:51Z","timestamp":1707507111000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/63241-congenital-methemoglobinemia-and-unstable-hemoglobin-variant-in-a-child-with-cyanosis"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,7,1]]},"references-count":13,"URL":"https:\/\/doi.org\/10.7759\/cureus.16081","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2021,7,1]]}}}