MPS I: The Importance of Early Diagnosis
Автор: Kim Angel IMPSN
Загружено: 2021-05-12
Просмотров: 1103
Rare diseases such as mucopolysaccharidosis type I (MPS I) disease, also known as Hurler syndrome, are difficult to identify because the symptoms can be wide-ranging.
It’s crucial to diagnose and treat children with MPS I early, before the disease causes permanent damage. If patients can receive a bone marrow or stem cell transplant by the age of two, the outcomes are much better.
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