Histidinemia: Difference between revisions
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Revision as of 16:00, 9 August 2012
| Histidinemia | |
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| Histidine | |
| ICD-10 | E70.8 |
| ICD-9 | 270.5 |
| OMIM | 235800 |
| DiseasesDB | 29669 |
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WikiDoc Resources for Histidinemia |
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Most recent articles on Histidinemia Most cited articles on Histidinemia |
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Powerpoint slides on Histidinemia |
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Evidence Based Medicine |
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Clinical Trials |
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Ongoing Trials on Histidinemia at Clinical Trials.gov Clinical Trials on Histidinemia at Google
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US National Guidelines Clearinghouse on Histidinemia
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Patient Resources / Community |
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Patient resources on Histidinemia Discussion groups on Histidinemia Patient Handouts on Histidinemia Directions to Hospitals Treating Histidinemia Risk calculators and risk factors for Histidinemia
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Healthcare Provider Resources |
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Causes & Risk Factors for Histidinemia |
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Continuing Medical Education (CME) |
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Overview
Histidinemia is a rare autosomal recessive metabolic disorder caused by a deficiency of the enzyme histidase. Histidase is needed for the metabolism of the amino acid histidine. Histidenemia is characterized by increased levels of histidine in blood, urine and cerebrospinal fluid, and decreased levels of the metabolite urocanic acid in blood, urine, and skin cells.