Patients are of almost normal height and do not show intellectual deficiency. The diagnosis is based on a certain number of clinical features. The authors report two unusual cases of hunterhurlers syndrome. A read is counted each time someone views a publication summary such as the title, abstract, and list of authors, clicks on a figure, or views or downloads the fulltext. The same is true for most diseases of genetic origin in which. Slitlamp views of the anterior segment show diffuse corneal stromal haze,a shallow anterior chamber,and a clear lens in the right a and left eyes b. Hurler scheie syndrome is the intermediate form of mucopolysaccharidosis type 1 mps1. Hurlerscheie syndrome is the intermediate form of mucopolysaccharidosis type 1 mps1.
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