Cargando…
Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Cause of Hepatomegaly
Multiple Acyl-CoA dehydrogenase deficiency (MADD) is an autosomal recessive disorder that can manifest with hepatic and muscular dysfunction. MADD can be fatal in neonates; however, late-onset MADD has a milder course and often becomes symptomatic during adulthood. A 20-year-old patient presented to...
| Autores principales: | , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer
2023
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166334/ https://www.ncbi.nlm.nih.gov/pubmed/37168503 http://dx.doi.org/10.14309/crj.0000000000001036 |