Hyperlysinemia: Difference between revisions
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Latest revision as of 18:23, 4 September 2012
Hyperlysinemia | |
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lysine | |
ICD-9 | 270.7 |
OMIM | 238700 |
DiseasesDB | 33215 |
MeSH | D020167 |
WikiDoc Resources for Hyperlysinemia |
Articles |
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Most recent articles on Hyperlysinemia Most cited articles on Hyperlysinemia |
Media |
Powerpoint slides on Hyperlysinemia |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Hyperlysinemia at Clinical Trials.gov Trial results on Hyperlysinemia Clinical Trials on Hyperlysinemia at Google
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Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Hyperlysinemia NICE Guidance on Hyperlysinemia
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Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Hyperlysinemia Discussion groups on Hyperlysinemia Patient Handouts on Hyperlysinemia Directions to Hospitals Treating Hyperlysinemia Risk calculators and risk factors for Hyperlysinemia
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Healthcare Provider Resources |
Causes & Risk Factors for Hyperlysinemia |
Continuing Medical Education (CME) |
International |
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Business |
Experimental / Informatics |
Hyperlysinemia is an autosomal recessive[1] metabolic disorder characterized by an abnormal increase of lysine in the blood, but appears to be benign. It can be associated with saccharopine dehydrogenase.
![](/images/a/a4/Autorecessive.jpg)
See also
References
- ↑ Sacksteder KA, Bier BJ, Morrell JC, Goodman BK, Geisbrecht BV, Cox RP, Gould SJ, Geraghty MT (2000). "Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia". American journal of human genetics. 66 (6): 1736–1743. doi:10.1086/302919. PMC 1378037. PMID 10775527. Unknown parameter
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