CNSHA

AcronymDefinition
CNSHACongenital Non-Spherocytic Haemolytic Anaemia
References in periodicals archive ?
Unlike the usual variant with episodic haemolysis on oxidative challenges, subjects with CNSHA demonstrate chronic haemolysis and splenomegaly.
Aunque las mutaciones se extienden a lo largo de la region codificadora del gen, existen unas pocas (4 de 56) que dan origen a la forma mas severa de deficiencia de la enzima, esto es, la que se encuentra asociada con CNSHA (clase 1) en los 160 aminoacidos del extremo N-terminal.
Although the mutations extend throughout the coding region of the gene, there exist few (4 of 56) that give origin to the most severe form of deficiency of the enzyme, this is, the one that is associated with CNSHA (type 1) in the 160 amino acids of the N-terminal end.