| Literature DB >> 16148061 |
Celia Perez-Cerda1, Judit García-Villoria, Rob Ofman, Pedro Ruiz Sala, Begoña Merinero, Julio Ramos, Maria Teresa García-Silva, Beatriz Beseler, Jaime Dalmau, Ronald J A Wanders, Magdalena Ugarte, Antonia Ribes.
Abstract
We describe three patients, from two Spanish families, with 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency, a recently described X-linked neurodegenerative inborn error of isoleucine metabolism. Two of them are males with severe lactic acidosis suggestive of a mitochondrial encephalopathy, and the third is a female who was less severely affected, suggesting skewed X-inactivation. Molecular studies revealed a new missense mutation, 740A-->G, in one family and a previously described mutation, 388C-->T, in the other, causing the amino acid substitutions N247S and R130C, respectively. Both male patients died, one of them despite treatment with an isoleucine-restricted diet, but the disease has remained stable in the female patient after 1 y of treatment.Entities:
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Year: 2005 PMID: 16148061 DOI: 10.1203/01.pdr.0000176916.94328.cd
Source DB: PubMed Journal: Pediatr Res ISSN: 0031-3998 Impact factor: 3.756