Neonatal hemolytic anemia due to the mother's rare RhD–/– phenotype: A case report

医学 输血医学 输血 贫血 输血疗法 外科 内科学
作者
Saeed Soleimany,Iraj Shokouhi,Mohammad Samare‐Najaf
标识
DOI:10.1002/pbc.30877
摘要

Pediatric Blood & CancerEarly View e30877 LETTER TO THE EDITOR Neonatal hemolytic anemia due to the mother's rare RhD–/– phenotype: A case report Saeed Soleimany, Saeed Soleimany Medical Laboratory Department, Kerman Blood Transfusion Center (KBTC), Iran Blood Transfusion Organisation (IBTO), Kerman, Iran Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Kerman Regional Blood Transfusion Center, Kerman, IranSearch for more papers by this authorIraj Shokouhi, Iraj Shokouhi Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Kerman Regional Blood Transfusion Center, Kerman, IranSearch for more papers by this authorMohammad Samare-Najaf, Corresponding Author Mohammad Samare-Najaf [email protected] orcid.org/0000-0002-1741-503X Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Kerman Regional Blood Transfusion Center, Kerman, Iran Department of Cell and Plasma Processing, Kerman Blood Transfusion Center, Iran Blood Transfusion Organisation, Kerman, Iran Correspondence Mohammad Samare-Najaf, Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Kerman Regional Blood Transfusion Center, Kerman, Iran. Email: [email protected]Search for more papers by this author Saeed Soleimany, Saeed Soleimany Medical Laboratory Department, Kerman Blood Transfusion Center (KBTC), Iran Blood Transfusion Organisation (IBTO), Kerman, Iran Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Kerman Regional Blood Transfusion Center, Kerman, IranSearch for more papers by this authorIraj Shokouhi, Iraj Shokouhi Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Kerman Regional Blood Transfusion Center, Kerman, IranSearch for more papers by this authorMohammad Samare-Najaf, Corresponding Author Mohammad Samare-Najaf [email protected] orcid.org/0000-0002-1741-503X Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Kerman Regional Blood Transfusion Center, Kerman, Iran Department of Cell and Plasma Processing, Kerman Blood Transfusion Center, Iran Blood Transfusion Organisation, Kerman, Iran Correspondence Mohammad Samare-Najaf, Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Kerman Regional Blood Transfusion Center, Kerman, Iran. Email: [email protected]Search for more papers by this author First published: 18 January 2024 https://doi.org/10.1002/pbc.30877Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES 1Li H-Y, Guo K. Blood group testing. Front Med. 2022; 9:827619. 10.3389/fmed.2022.827619 Google Scholar 2Floch A, Siegel DL, Westhoff CM. Rh and LW blood group antigens. In: Rossi's Principles of Transfusion Medicine. John Wiley & Sons Ltd.; 2022: 100-108. 10.1002/9781119719809.ch10 Google Scholar 3Ye L, Li M, Yang Q, Zhu Z. RHD alleles contributing to serologically weak D phenotypes in China: a single-centre study over 10 years. Vox Sang. 2022; 117(7): 949-957. 10.1111/vox.13275 CASPubMedWeb of Science®Google Scholar 4Ćutuk R, Hromić-Jahjefendić A. RhD detection in transfusion medicine. Bioengineering Stud. 2022; 3(2): 21-34. 10.37868/bes.v3i2.id238 Google Scholar 5Moise KJ Jr, Uhl L. RhD alloimmunization in pregnancy: overview. UpToDate; 2022. Google Scholar 6Elsayid M, Al Qahtani FS, Al Qarni AM, Almajed F, Al Saqri F, Qureshi S. Determination of the frequency of the most immunogenic Rhesus antigens among Saudi donors in King Abdulaziz Medical City - Riyadh. J Nat Sci Biol Med. 2017; 8(1): 56. 10.4103/0976-9668.198361 PubMedGoogle Scholar 7Gundrajukuppam DK, Vijaya SBK, Rajendran A, Sarella JD. Prevalence of principal Rh blood group antigens in blood donors at the blood bank of a tertiary care hospital in Southern India. J Clin Diagnostic Res. 2016; 10(5): EC07. CASPubMedGoogle Scholar 8He Y, Gao W, Li Y, Xu C, Wang Q. A single-center, retrospective analysis of 17 cases of hemolytic disease of the fetus and newborn caused by anti-M antibodies. Transfusion (Paris). 2023; 63(3): 494-506. 10.1111/trf.17249 CASPubMedWeb of Science®Google Scholar 9Mia MM, Islam MS, Hussain RF, Hoque S. Haemolytic disease of the newborn. KYAMC J. 2023; 14(01): 54-56. 10.3329/kyamcj.v14i01.67510 Google Scholar 10Sahoo D, Anuragaa S, Abhishekh B. Anti-C causing severe hemolytic disease of the fetus and newborn: a rare case report. Immunohematology. 2023; 39(1): 11-14. CASPubMedGoogle Scholar 11Flatt JF, Musa RH, Ayob Y, et al. Study of the D–phenotype reveals erythrocyte membrane alterations in the absence of RHCE. Br J Haematol. 2012; 158(2): 262-273. 10.1111/j.1365-2141.2012.09149.x CASPubMedWeb of Science®Google Scholar 12Ghesquière L, Garabedian C, Coulon C, et al. Management of red blood cell alloimmunization in pregnancy. J Gynecol Obstet Hum. 2018; 47(5): 197-204. CASGoogle Scholar 13Moise KJ Jr. Management of rhesus alloimmunization in pregnancy. Obstet Gynecol. 2002; 100(3): 600-611. 10.1097/00006250-200209000-00032 PubMedGoogle Scholar 14Samareh Salavati Pour M, Soleimany S, Ghasemimehr N, Mirzaee Khalilabadi R. A case report of a rare Rh phenotype: D—. Indian J Hematol Blood Transfus. 2019; 35: 402-404. 10.1007/s12288-019-01089-7 PubMedWeb of Science®Google Scholar Early ViewOnline Version of Record before inclusion in an issuee30877 ReferencesRelatedInformation
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