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<title>OWL: OCOSH Classification/Systemic Disorders</title>
<link>http://www.orthopaedicweblinks.com</link>
<description>Systemic disorders that affect the musculoskeletal system
&lt;br&gt;ICD-10 Code M36 Systemic disorders of connective tissue in diseases classified elsewhere
&lt;br&gt;SNOMED-CT Term Systemic disease (finding) Concept ID: 56019007
&lt;br&gt;No equivalent MeSH term or unique ID
</description>
<language>en-us</language>
<lastBuildDate>Mon May 16 2011 00:15:00 GMT</lastBuildDate>
<copyright>Copyright 2005 OWL Inc.</copyright>
<managingEditor>orthopaedicweblinks@gmail.com (Christian Veillette)</managingEditor>
<webMaster>orthopaedicweblinks@gmail.com (OWL Inc.)</webMaster>
<item>
<title>2011 Distinguishing fibromyalgia from rheumatoid arthritis and systemic lupus in clinical questionnaires</title>
<link>http://www.orthopaedicweblinks.com/Detailed/18087.html</link>
<description>Conclusions
A combination of 2 questions (&quot;tenderness to touch&quot; and &quot;difficulty sitting for 45 minutes&quot;) plus pain in the lower back, neck, hands and arms, may be useful in the construction of clinical questionnaires aimed at patients with musculoskeletal pain. This combination provided a correct diagnosis in 97% of subjects, with only 7 of 253 subjects misclassified.&lt;br&gt;
Distinguishing fibromyalgia from rheumatoid arthritis and systemic lupus in clinical questionnaires: an analysis of the revised fibromyalgia impact questionnaire (FIQR) and its variant the symptom impact questionnaire (SIQR) along with pain locations
Ronald Friend and Robert M Bennett
Arthritis Research &amp; Therapy 2011, 13:R58 </description>
<pubDate>2011-04-13 00:15:00 GMT</pubDate>
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<author>Friend and Bennett</author>
</item><item>
<title>Congenital and Metabolic Diseases</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10315.html</link>
<description>There is no single unifying trait for these disorders.   Some have their genetic defect well characterized.  Others are still waiting for the discovery of the gene or genes which are damaged.  The diagnosis requires careful clinical laboratory evaluation and may require testing for enzymes that are only available in research laboratories.  Biopsy diagnosis may play an important role, not only in establishing the diagnosis, but providing fresh tissue for molecular and enzyme studies.
Acrodermatitis Enteropathica
Alagille Syndrome
Alkaptonuria (Ochronosis)
Alpha-1-Antitrypsin Deficiency
Alport Syndrome
Amyloid
Bannayan-Zonana Syndrome
Canavan Disease
Common Variable Immunodeficiency
Cowden Syndrome
Cystic Fibrosis
Diabetes Insipidus
Down Syndrome (Trisomy 21)
Ectodermal Dysplasia
Ehlers-Danlos Disease
Fabry Disease
Fucosidosis
Galactosemia
Gaucher Disease
Glucagonoma
Gout
Juvenile Hyaline Fibromatosis (Murray-Puretic Syndrome)
Mucopolysaccharidoses
Necrolytic Migratory Erythema
Neurofibromatosis
Ochronosis (Alkaptonuria)
Osteogenesis Imperfecta
Porphyria
Proteus Syndrome
Pseudogout
Pseudoporphyria
Refsum&#039;s Disease
Restrictive Dermopathy
Retinitis Pigmentosa
Rubinstein-Taybi Syndrome
Scurvy (Vitamin C Deficiency)
Shwachman-Diamond Syndrome
Syndrome of Inappropriate Anti-Diuretic Hormone (SIADH)
Tuberous Sclerosis
von Hippel-Lindau Disease
Williams Syndrome</description>
<pubDate>2006-11-29 00:15:00 GMT</pubDate>
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<author></author>
</item><item>
<title>Musculoskeletal involvement in systemic lupus erythematosus Orthopaedia</title>
<link>http://www.orthopaedicweblinks.com/Detailed/15297.html</link>
<description>Systemic lupus erythematosus (SLE) is an inflammatory autoimmune disease associated with antinuclear antibody (ANA) production.  Clinical manifestations of SLE can involve nearly every organ system, including the skin, heart, lungs, kidneys, nervous system, blood, and musculoskeletal system.  Patients with SLE may initially present to the orthopedist because joint pain is one of the earliest and most common symptoms of SLE, occurring in 50-95% of patients.</description>
<pubDate>2009-07-07 00:15:00 GMT</pubDate>
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<author>Not Available</author>
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