Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Alloimmunization to a high frequency Rh antigen].

Medicina - 1 Jan 2006

Cotorruelo Carlos, Biondi Claudia, Borras Silvia Garcia, Racca Liliana, Brunetti Daniel, Di Monaco Rene, Racca Amelia

Abstract excerpt

We report the case of a pregnant woman sensitized with a panreactive anti-Rh17 alloantibody. Patient's red blood cells showed a partial deletion of Rh antigens, which was responsible for the alloimmunization. An autotransfusion program was instrumented so as to cover possible demands. Molecular analysis of the RH locus showed the presence of a hybrid RHCE-D(5-7)-CE allele that gave origin to the deleted phenotype.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Phenotype
Share to Pregnancy
Share to Isoantibodies

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Genotype

Share to Pregnancy Complications, Hematologic

Share to Rh-Hr Blood-Group System

Share to Rh Isoimmunization

Source

Identifiers

PMID: 16555729

Genes

RHCE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Alloimmunization to a high frequency Rh antigen].PMID 16555729Read ↗

Sensitization to multiple rh antigens by transfusion of random donor platelet concentrates in a -D- phenotype patient.Semantic proximity Read ↗

A case of anti-Rh17 (anti-Hro) antibody in D··phenotype, a rare alloimmunization complicating transfusion management.Semantic proximity Read ↗

Anti-Rh39--a "new" specificity Rh system antibody.Semantic proximity Read ↗

D--phenotype due to RHD-RHCE hybrid transcript in a case of severe haemolytic disease of newborn with anti-Rh 17(Hrₒ) antibodies.Semantic proximity Read ↗

[Progress in investigations of blood group antigen functions of red cells].Semantic proximity Read ↗

ceRA: an RH allele variant producing a new rare blood.Semantic proximity Read ↗

Association of multispecific red blood cell alloimmunization with HLA-Class II variants is related to Rh phenotypes.Semantic proximity Read ↗

MAR, a novel high-incidence Rh antigen revealing the existence of an allelic sub-system including Cw (Rh8) and Cx (Rh9) with exceptional distribution in the Finnish population.Semantic proximity Read ↗

[Study on the Production of Anti-D and Anti-E Mixed Antibodies by Alloimmunization in RhD Variant Type33 Recipients].Semantic proximity Read ↗

Hemolytic disease of the fetus and newborn caused by anti-Hr0 in a 27-year-old female with Dc- phenotype: A case report.Semantic proximity Read ↗

[Sr(a), a "private" thrombocyte alloantigen as a cause of neonatal alloimmune thrombocytopenia].Semantic proximity Read ↗

[Detection of defects in components of antigen I and its significance in transfusiology].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.