Ethylmalonic encephalopathy: phenotype-genotype description and review of its management
Neurologia (Engl Ed)
.
2021 Nov-Dec;36(9):729-731.
doi: 10.1016/j.nrleng.2021.01.003.
Epub 2021 Jul 15.
Authors
N Cardelo Autero
1
,
A M Cordón Martínez
2
,
J M Ramos-Fernández
3
Affiliations
1
Servicio de Pediatría, Hospital Regional Universitario Materno-Infantil de Málaga, Málaga, Spain.
2
Servicio de Pediatría (lactantes), Hospital Regional Universitario Materno-Infantil de Málaga, Málaga, Spain.
3
Sección de Neurología Pediátrica, Grupo IBIMA, Servicio de Pediatría, Hospital Regional Universitario Materno-Infantil de Málaga, Málaga, Spain. Electronic address:
[email protected]
.
PMID:
34274260
DOI:
10.1016/j.nrleng.2021.01.003
No abstract available
Publication types
Letter
MeSH terms
Brain Diseases, Metabolic, Inborn*
Genotype
Humans
Phenotype
Purpura*
Supplementary concepts
Ethylmalonic encephalopathy