Hurler syndrome: Difference between revisions
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==Case Studies== | ==Case Studies== | ||
[[Hurler syndrome case study one|Case #1]] | [[Hurler syndrome case study one|Case #1]] | ||
{{Endocrine, nutritional and metabolic pathology}} | {{Endocrine, nutritional and metabolic pathology}} |
Revision as of 21:05, 25 February 2013
For patient information click here Template:DiseaseDisorder infobox
Hurler Syndrome Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Hurler syndrome On the Web |
American Roentgen Ray Society Images of Hurler syndrome |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Alpha-L-iduronidase deficiency; Hurler-Pfaundler syndrome, Hurler-Hunter syndrome, Hunter’s syndrome, Johnie McL disease, Pfaundler-Hurler disease, Pfaundler-Hurler syndrome, Sheldon-Ellis syndrome, Thompson’s syndrome, Hurler's disease, Hurler's syndrome
Overview
Classification
Pathophysiology
Causes
Differentiating Hurler syndrome from other Diseases
Epidemiology and Demographics
Risk Factors
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | EKG | Echocardiography or Ultrasound | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Cost-Effectiveness of Therapy | Future or Investigational Therapies