Alma Mater Studiorum - Forlì


Home page
Le collezioni
La scuola
Il progetto
I collaboratori
Gli sponsor
Il laboratorio
Regole e normative
Per contattarci
Copyright


login
password
ho dimenticato la password
mi voglio iscrivere

ceci n'est pas une pomme
 
previous precipitation - collezione «Medicina: Ematologia: Talassemie e trapianto del midollo osseo» - Deborah Olmi next
Cerca   nella collezione  

Medicina: Ematologia: Talassemie e trapianto del midollo osseo

English
precipitation clicca per ingrandire
Attestation 3
Part of speech Noun
Grammatical label Countable
Definition The lack of b-globin chain components in b-thalassemia trait is usually sufficiently compensated for by increased b-globin chain expression of the normal allele and by an increase in red cell production. The short b gene products and free a-chains, remaining in excess after formation of the hemoglobin tetramers, are usually efficiently eliminated by proteolytic cleavage and are only responsible for a minor degree of ineffective erythropoiesis, which is usually well tolerated and not associated with hemolysis. However, chain precipitation and cell membrane damage, leading to ineffective erythropoiesis and hemolysis, may be present in patients heterozygous for b-thalassemia, when the trait is induced by mutations located on the third exon of the gene.
Definition source Giordano, PC., et al. (1998). ‘Phenotype variability of the dominant beta-thalassemia induced in four Dutch families by the rare cd121 (G-->T) mutation’. Annals of Hematology 77(6):249-55. (RISCEN92)
Context The precipitation starts already in the poly-chromatophilic erythroblasts and is maximal in the most mature cells. Precipitation of unbound a-chains occurs in the cytoplasm, but apparently takes place also within the nuclei. The latter event is probably connected with the disturbed erythroblast cycle in thalassemia, namely their arrest in phase Gl and the accumulation of glycogen. - The a-chain precipitation is followed by severe impairment of the electrolyte balance and by abundant release of free radicals which attack all cellular constituents (membranes, hemoglobin, enzymes etc.) and lead to premature death of the cell.
Context source Loukopoulos, D. (1991). ‘Thalassemia: genotypes and phenotypes’. Annals of Hematology 62(4):85-94. Review. (RISCEN96)
Subject field Haemopoiesis
Sub-field (level 1) Thalassemias
Related concept Globin synthesis imbalance
it Precipitazione
Reliability code 3



SSLMIT - Scuola Superiore di Lingue Moderne per Interpreti e Traduttori  &  MIT - Management Innovative Tools S.p.A. - Powered by : Powered by DynaMIT