Macro-AST: misleading finding in an adolescent with MCAD-deficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,General Medicine
Link
http://link.springer.com/article/10.1186/1471-230X-12-119/fulltext.html
Reference9 articles.
1. Grosse SD, Khoury MJ, Greene CL, Crider KS, Pollitt RJ: The epidemiology of medium chain acyl-CoA dehydrogenase deficiency: an update. Genet Med. 2006, 8 (4): 205-212. 10.1097/01.gim.0000204472.25153.8d.
2. Schatz UA, Ensenauer R: The clinical manifestation of MCAD deficiency: challenges towards adulthood in the screened population. J Inherit Metab Dis. 2010, 33 (5): 513-520. 10.1007/s10545-010-9115-5.
3. Caropreso M, Fortunato G, Lenta S, Palmieri D, Esposito M, Vitale DF, Iorio R, Vajro P: Prevalence and long-term course of macro-aspartate aminotransferase in children. J Pediatr. 2009, 154 (5): 744-748. 10.1016/j.jpeds.2008.11.010.
4. Fortunato G, Iorio R, Esposito P, Lofrano MM, Vegnente A, Vajro P: Macroenzyme investigation and monitoring in children with persistent increase of aspartate aminotransferase of unexplained origin. J Pediatr. 1998, 133 (2): 286-289. 10.1016/S0022-3476(98)70238-0.
5. Litin SC, O'Brien JF, Pruett S, Forsman RW, Burritt MF, Bartholomew LG, Baldus WP: Macroenzyme as a cause of unexplained elevation of aspartate aminotransferase. Mayo Clin Proc. 1987, 62 (8): 681-687.
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