Voiko veriryhmän reesus muuttua?

Seuraa 
Viestejä45973
Liittynyt3.9.2015

Löysin vanhan neuvolakorttini ja siihen oli merkitty veriryhmäksi A rh -, verenluovutuksessa käydessäni sain kortin jossa se oli A rh +.

Voiko se tosiaan muuttunut vai onko tässä sattunut "painovirhepaholainen"?

Kommentit (1)

rosewater
Seuraa 
Viestejä1231
Liittynyt1.4.2007
Etori
Löysin vanhan neuvolakorttini ja siihen oli merkitty veriryhmäksi A rh -, verenluovutuksessa käydessäni sain kortin jossa se oli A rh +.

Voiko se tosiaan muuttunut vai onko tässä sattunut "painovirhepaholainen"?


Mielenkiintoinen kysymys. Vastaus on, että kyllä voi, tai oikeammin määrityksen tulos voi vaihdella. RhD on geneettisesti varsin heterogeeninen ja näin ollen eri serologisilla menetelmillä voi tulla erilaisia tuloksia. Harvinaista tämä toki on ja nykyisin tyypitys tehdään usein genotyyppaamalla eikä serologisesti. Lisäksi on olemassa tietysti (lähes häviävän pieni) kimeerisyyden mahdollisuus.

Wagner FF, Frohmajer A, Flegel WA: RHD positive haplotypes in D negative Europeans.

BMC Genet. 2001;2:10. Epub 2001 Jul 16.

BACKGROUND: Blood group genotyping is increasingly utilized for prenatal diagnosis and after recent transfusions, but still lacks the specificity of serology. In whites, the presence of antigen D is predicted, if two or more properly selected RHD-specific polymorphism are detected. This prediction must fail, if an antigen D negative RHD positive allele is encountered. Excluding RHDpsi and CdeS frequent only in individuals of African descent, most of these alleles are unknown and the population frequency of any such allele has not been determined. METHODS: We screened 8,442 antigen D negative blood donations by RHD PCR-SSP. RHD PCR positive samples were further characterized by RHD exon specific PCR-SSP or sequencing. The phenotype of the identified alleles was checked and their frequencies in Germans were determined. RESULTS: We detected 50 RHD positive samples. Fifteen samples harbored one of three new Del alleles. Thirty samples were due to 14 different D negative alleles, only 5 of which were previously known. Nine of the 14 alleles may have been generated by gene conversion in cis, for which we proposed a mechanism triggered by hairpin formation of chromosomal DNA. The cumulative population frequency of the 14 D negative alleles was 1:1,500. Five samples represented a D+/- chimera, a weak D and three partial D, which had been missed by routine serology; two recipients transfused with blood of the D+/- chimera donor became anti-D immunized. CONCLUSION: The results of this study allowed to devise an improved RHD genotyping strategy, the false-positive rate of which was lower than 1:10,000. The number of characterized RHD positive antigen D negative and Del alleles was more than doubled and their population frequencies in Europe were defined.

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