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<title>OWL: Orthopedic Topics/Systemic Disorders</title>
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<description>Orthopedic systemic disorders and metabolic bone diseases</description>
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<lastBuildDate>Sun Apr 20 2008 14:25:45 GMT</lastBuildDate>
<copyright>Copyright 2005 OWL Inc.</copyright>
<managingEditor>orthopaedicweblinks@gmail.com (Christian Veillette)</managingEditor>
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<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 14:25:45 GMT</pubDate>
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