https://www.selleckchem.com/products/XAV-939.html
Imerslund-Gräsbeck syndrome is a rare genetic disease characterised by vitamin B deficiency and proteinuria. A 4-year old Sri Lankan boy presented with gradually worsening difficulty in walking for two weeks duration. He was previously diagnosed and managed as having non-transfusion-dependent α-thalassaemia based on the presence of hypochromic microcytic anaemia, haemoglobin H inclusion bodies in the blood film and compound heterozygous α-thalassaemia genotype with a gene deletion. However, his transfusion requirement increased over the
Curtir
Comentario
Compartilhar
