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Hurler-Scheie Syndrome
Alpha L iduronidase , Mucopolysaccharidois, MPS H/S
Hurler-Scheie is a lysosomal storage disease (Mucopolysaccharide type I). The symptoms of this condition are less severe than Hurler’s but more severe than Sheie’s. Onset for this condition is generally around 3-8 years and presents with mild facial deformities, corneal clouding, joint stiffness and shortness of stature. Hydrocephaly and intellectual disability may be present.
Useful Links
This national organisation website provides a comprehensive view of this disorder:
This national organisation website provides a brief view of all the mucopolysaccharide disorders:
This website provides information on mucopolysaccharide disorders such as causes, diagnosis, treatment, behavioural complications and the issues that affect families:
A local New Zealand organisation website providing information on the disorder, the organisation, research and resources:
Support Groups
Person/Organisation:
Lysosomal Diseases New Zealand
Postal Address:
125 Cuba Street
Petone
Lower Hutt City
Phone Number:
04 566 7707
Fax Number:
04 566 7717
Email:
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