Hunter syndrome: Difference between revisions
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==[[Hunter syndrome pathophysiology|Pathophysiology]]== | ==[[Hunter syndrome pathophysiology|Pathophysiology]]== | ||
==[[Hunter syndrome differential diagnosis|Differentiating Hunter syndrome from other Diseases]]== | ==[[Hunter syndrome differential diagnosis|Differentiating Hunter syndrome from other Diseases]]== | ||
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==[[Hunter syndrome risk factors|Risk Factors]]== | ==[[Hunter syndrome risk factors|Risk Factors]]== | ||
==[[Hunter syndrome natural history, complications and prognosis|Natural History, Complications and Prognosis]]== | ==[[Hunter syndrome natural history, complications and prognosis|Natural History, Complications and Prognosis]]== |
Revision as of 18:24, 26 February 2013
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Hunter syndrome Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Hunter syndrome On the Web |
American Roentgen Ray Society Images of Hunter syndrome |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Iduronate-2-sulfatase deficiency; MPS II; mucopolysaccharidosis II; iduronate sulphatase deficiency
Overview
Historical Perspective
Pathophysiology
Differentiating Hunter syndrome from other Diseases
Epidemiology and Demographics
Risk Factors
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Cost-Effectiveness of Therapy | Future or Investigational Therapies
Case Studies
Related Chapters
Template:Endocrine, nutritional and metabolic pathology