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

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
我是老大应助科研通管家采纳,获得10
刚刚
tiptip应助科研通管家采纳,获得10
刚刚
刚刚
肥猪发布了新的文献求助10
1秒前
英俊的铭应助安逸采纳,获得10
1秒前
凌尘完成签到 ,获得积分10
3秒前
Lucas应助十字星采纳,获得30
4秒前
CipherSage应助独特亦旋采纳,获得10
5秒前
6秒前
6秒前
传奇3应助好心情采纳,获得10
7秒前
bkagyin应助海风吹过小镇采纳,获得10
8秒前
领导范儿应助litianchi采纳,获得10
8秒前
干净的琦应助蓝天采纳,获得30
9秒前
科目三应助wuhao采纳,获得10
9秒前
9秒前
whoknowsname发布了新的文献求助10
10秒前
10秒前
11秒前
11秒前
lize5493发布了新的文献求助10
12秒前
佳仪完成签到 ,获得积分10
12秒前
14秒前
朴BOSS发布了新的文献求助10
14秒前
xibei发布了新的文献求助10
15秒前
16秒前
陈宝玉发布了新的文献求助10
17秒前
17秒前
十字星完成签到,获得积分20
18秒前
生动依凝发布了新的文献求助10
18秒前
19秒前
19秒前
ronaldo发布了新的文献求助10
22秒前
23秒前
一一发布了新的文献求助10
23秒前
wuhao发布了新的文献求助10
23秒前
二三发布了新的文献求助10
23秒前
生动依凝完成签到,获得积分10
24秒前
咖啡完成签到,获得积分10
27秒前
独特亦旋发布了新的文献求助10
27秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Salmon nasal cartilage-derived proteoglycan complexes influence the gut microbiota and bacterial metabolites in mice 2000
The Composition and Relative Chronology of Dynasties 16 and 17 in Egypt 1500
Cowries - A Guide to the Gastropod Family Cypraeidae 1200
Hemispherical Resonator Gyro: Status Report and Test Results 800
ON THE THEORY OF BIRATIONAL BLOWING-UP 666
Signals, Systems, and Signal Processing 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6383223
求助须知:如何正确求助?哪些是违规求助? 8195469
关于积分的说明 17327739
捐赠科研通 5436876
什么是DOI,文献DOI怎么找? 2875358
邀请新用户注册赠送积分活动 1852160
关于科研通互助平台的介绍 1696598