Short stature is characteristic of patients with
mucopolysaccharidosis (MPS) diseases. For children with skeletal dysplasias,
such as MPS, it is important to know the natural history of growth. An
understanding of the natural growth pattern in each MPS disease provides a
measurement to which treatments can be compared, as well as data which can help
families and providers make individualized decisions about growth promoting
treatments. Multiple advancements have been made in the treatment of MPS with
both hematopoietic cell transplantation (HCT) and enzyme replacement therapy
(ERT). The long term benefit of these treatments on growth is unknown. This
article will review the published data on growth in children with MPS, and
describe preliminary data on the use of human growth hormone (hGH) in children
with MPS.