Study of patients and carriers with 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: Difficulties in the diagnosis

Clinical Biochemistry - Tập 42 - Trang 27-33 - 2009
Judit García-Villoria1, Aleix Navarro-Sastre1, Carme Fons2, Celia Pérez-Cerdá3, Antonio Baldellou4, Miguel Ángel Fuentes-Castelló5, Inmaculada González6, Arturo Hernández-Gonzalez7, Cristina Fernández1, Jaume Campistol2, Carina Delpiccolo8, Nuria Cortés8, Angel Messeguer8, Paz Briones1,8, Antonia Ribes1
1Sección de Errores Congénitos del Metabolismo (IBC), Servicio de Bioquímica y Genética Molecular and CIBER de Enfermedades Raras (CIBERER), Hospital Clínic, Barcelona, Spain
2Servicio de Neurología. Hospital Sant Joan de Déu and CIBER de Enfermedades Raras (CIBERER), Barcelona, Spain
3Centro de Diagnóstico de Enfermedades Moleculares, Universidad Autónoma de Madrid, and CIBER de Enfermedades Raras (CIBERER), Madrid, Spain
4Unidad de Enfermedades Metabólicas. Hospital Miguel Server, Zaragoza, Spain
5Servicio de Pediatría. Hospital General Universitari d'Elx, Alicante, Spain
6Sección Metabolopatías. Centro de Bioquímica y Genética Clínica. Hospital Virgen de la Arrixaca, Murcia, Spain
7Servicio de Pediatría. Hospital Universitario Puerta del Mar. Cádiz, Spain
8Department of Biological Organic Chemistry, IIQAB (CSIC), Barcelona, Spain

Tài liệu tham khảo

Zschocke, 2000, Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: a novel inborn error of branched-chain fatty acid and isoleucine metabolism, Pediatr. Res., 48, 852, 10.1203/00006450-200012000-00025 Yan, 1997, An intracellular protein that binds amyloid-b peptide and mediates neurotoxicity in Alzheimer's disease, Nature, 389, 689, 10.1038/39522 Lustbader, 2004, ABAD directly links Aβ to mitochondrial toxicity in Alzheimer's disease, Science, 304, 448, 10.1126/science.1091230 Yang, 2005, Multiple functions of type 10 17β-hydroxysteroid dehydrogenase, Trends Endocrinol. Metab., 16, 167, 10.1016/j.tem.2005.03.006 Murakami, 2007, Cytoprotective role of mitochondrial amyloid β peptide-binding alcohol dehydrogenase against a cytotoxic aldehyde, Neurobiol. Aging Poll-The, 2004, Spastic diplegia and periventricular white matter abnormalities in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, a defect of isoleucine metabolism: differential diagnosis with hypoxic-ischemic brain diseases, Mol. Genet. Metab., 81, 295, 10.1016/j.ymgme.2003.11.013 Ensenauer, 2002, Clinical variability in 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency, Ann. Neurol., 51, 656, 10.1002/ana.10169 Olpin, 2002, 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency in a 23 year old man, J. Inherit. Metab. Dis., 25, 477, 10.1023/A:1021251202287 Sass, 2004, 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: impaired catabolism of isoleucine presenting as neurodegenerative disease, Brain Dev., 26, 12, 10.1016/S0387-7604(03)00071-8 Sutton, 2003, 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency, J. Inherit. Metab. Dis., 26, 69, 10.1023/A:1024083715568 Perez-Cerdá, 2005, 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: an X-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease, Pediatr. Res., 58, 488, 10.1203/01.pdr.0000176916.94328.cd Cazorla, 2007, Neuroimage findings in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, Pediatr. Neurol., 36, 264, 10.1016/j.pediatrneurol.2006.11.014 Ofman, 2003, 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency is caused by mutations in the HADH2 gene, Am. J. Hum. Genet., 72, 1300, 10.1086/375116 Lenski, 2007, The reduced expression of the HADH2 protein causes X-linked mental retardation, choreoathetosis, and abnormal behaviour, Am. J. Hum. Genet., 80, 372, 10.1086/511527 Miller, 1998, Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21–p11.22 that escapes X inactivation, Genetics, 95, 8709 Ribes, 1992, Significance of bound glutarate in the diagnosis of glutaric aciduria type I, J. Inherit. Metab. Dis., 15, 367, 10.1007/BF02435978 Wanders, 2001, 2-methyl.3.hydroxybutyryl-CoA dehydrogenase deficiency, a new disorder of isoleucine and branched-chain fatty acid degradation: studies on the forward and reverse reactions, New Avenues of Research in Fatty Acid Oxidation and Ketone Body Metabolism, 59 Rosa, 2005, Inhibition of energy metabolism by 2-methylacetoacetate and 2-methy-3-hydroxybutyrate in cerebral cortex of developing rats, J. Inherit. Metab. Dis., 28, 501, 10.1007/s10545-005-0501-3 Mammer, 1976, Demonstration of a new mammalian isoleucine catabolic pathway yielding an R series o metabolites, Biochem. J., 160, 417, 10.1042/bj1600417a Chelly, 1986, De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy, Hum. Genet., 74, 193, 10.1007/BF00282093 Zschocke, 2007, Neurodegeneration in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency is unrelated to enzyme function, J. Inherit. Metab. Dis., 30, 42