A rare combination of common childhood complaints could indicate Hunter syndrome (MPS II), a rare, multisystemic and progressive genetic disease.


Hunter syndrome is a rare, progressive genetic disease

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This website has been developed as an educational resource for healthcare professionals interested in learning more about Hunter syndrome, also known as mucopolysaccharidosis type II (MPS II).

*Consider the importance of early assessment, diagnosis, and follow-up by a specialist

Silas Silas 1.5 years Silas 3 years Silas 5 years
Silas Silas 1.5 years Silas 3 years Silas 5 years

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