small baby in hospital bed very ill
An infant with Hurler syndrome; a deficiency in the alpha-L-iduronidase enzyme. Apha-L-iduronidase is responsible for the break down of glycosaminoglycans - a component of connective tissues within the body. With the deficiency of this enzyme, the stores of glycosaminoglycan accumulate. This patient is presented with hepatosplenomegaly (enlarged live
Size: 3393px × 5100px
Photo credit: © Medicshots / Alamy / Afripics
License: Licensed
Model Released: No
Keywords: abdomen, alpha--iduronidase, baby, bone, child, deficiency, disease, diseases, enzyme, gargoylism, glycosaminoglycans, growth, hepatospleenomegally, hospital, hurler, illness, infant, jaundice, large, liver, marking, marrow, mucopolysaccharide, mucopolysaccharidosis, red, small, spleen, stomach, syndrome, transplant, yellow
