Mapping Rare Erythrocyte Phenotypes in Morocco: A Tool to Overcome Transfusion Challenges

Benahadi A.; Boulahdid S.; Adouani B.; Laouina A.; Mokhtari A.; Soulaymani A.; Hajjout K.; Benajiba M.; Alami R.

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Mapping Rare Erythrocyte Phenotypes in Morocco: A Tool to Overcome Transfusion Challenges

机译：在摩洛哥映射稀有的红细胞表型：克服输血挑战的工具

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The aim of this research is to search for the distribution of blood groups in all the regions of Morocco. This study, done for the first time, aimed to provide the frequency of the Rhesus system and Kell (K) in more than 55000 blood donors from nine different regions around the country. In addition, the frequency of the Cellano, Duffy, Kidd, and MNS blood antigens was searched for 500 blood donors from the Rabat’s region. Frequency of blood donors with rare blood groups was characterized for the first time in the country and compared to results found from other populations.

机译：本研究的目的是搜索摩洛哥所有地区的血型分布。本研究首次完成，旨在为恒河系统和凯尔（k）的频率提供来自该国九个不同地区的55000多个献血者。此外，Cellano，Duffy，Kidd和MNS血脂的频率被搜查了来自拉巴特区域的500份献血者。血液供体的频率在该国首次表现为第一次，并与来自其他人群的结果相比。

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《Journal of Transfusion》 |2014年第1期|共页
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Benahadi A.; Boulahdid S.; Adouani B.; Laouina A.; Mokhtari A.; Soulaymani A.; Hajjout K.; Benajiba M.; Alami R.;
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1. Genotyping versus phenotyping of non-ABO erythrocyte antigens in patients with the Mediterranean hemopathic syndromes: Effect of transfusion therapy [J] . Eman NasrEldin, Safaa A. A. Khaled, Nada O. Abdelhameed, PLoS One . 2021,第7期

机译：地中海血液肿瘤综合征患者非ABO红细胞抗原的基因分型与表型分类：输血治疗的影响
2. The rare codon 24 (T>A) (beta+) mutation in association with the common codon 39 (C> T) (beta0) mutation causes transfusion-dependent beta-thalassemia in a Moroccan patient. [J] . Agouti I, Bennani M, Levy N, Hemoglobin: International Journal for Hemoglobin Research . 2009,第2期

机译：罕见密码子24（T> A）（beta +）突变与普通密码子39（C> T）（beta0）突变相关，导致摩洛哥患者输血依赖的β地中海贫血。
3. Alterations of the erythrocyte membrane proteome and cytoskeleton network during storage - a possible tool to identify autologous blood transfusion [J] . NikolovskiZ., DeLaTorreC., ChivaC., Drug testing and analysis . 2012,第11a12期

机译：储存过程中红细胞膜蛋白质组和细胞骨架网络的变化-一种可能的工具来识别自体输血
4. RAMEDIS- rare metabolic diseases publishing tool for genotype-phenotype correlation. [C] . Mischke U, Scholz U, Toepel T, MEDINFO . 2001

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5. Development and validation of transfusion risk: Understanding scoring tool (TRUST) to stratify cardiac surgery patients according to their blood transfusion needs. [D] . Alghamdi, Abdullah A. 2005

机译：制定和确认输血风险：了解评分工具（TRUST），根据心脏手术患者的输血需求对其进行分层。
6. Mapping Rare Erythrocyte Phenotypes in Morocco: A Tool to Overcome Transfusion Challenges [O] . A. Benahadi, S. Boulahdid, B. Adouani, 2014

机译：映射摩洛哥罕见的红细胞表型：克服输血挑战的工具
7. P-Null Phenotype Due to a Rare Frame-Shift Mutation and with Allo-Anti-PP1Pk Causing a Severe Hemolytic Transfusion Reaction: A Case Report with Clinical Management [O] . Ashish N. Kanani, Snehal B. Senjaliya, Manisha M. Rajapara, 2021

机译：由于罕见的帧间移位突变和含有血栓溶膜输血反应的罕见血栓输血反应，P-禁止表型：临床管理的病例报告

Mapping Rare Erythrocyte Phenotypes in Morocco: A Tool to Overcome Transfusion Challenges

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