Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency

समान संसाधन

• A Case of Late‐onset Riboflavin Responsive Multiple acyl‐CoA Dehydrogenase Deficiency with Novel Mutations in ETFDH Gene
  द्वारा: Zhao, Zhang‐Ning, और अन्य
  प्रकाशित: (2012)
• Rhabdomyolysis and acute encephalopathy in late onset medium chain acyl-CoA dehydrogenase deficiency.
  द्वारा: Ruitenbeek, W, और अन्य
  प्रकाशित: (1995)
• Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations
  द्वारा: Chen, Wei, और अन्य
  प्रकाशित: (2019)
• Long-term outcomes of a patient with late-onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutations in ETFDH: A case report
  द्वारा: Wang, Juan, और अन्य
  प्रकाशित: (2018)
• Neonatal-onset multiple acyl-CoA dehydrogenase deficiency (MADD) in the ETFDH gene: A case report and a literature review
  द्वारा: Ding, Meijuan, और अन्य
  प्रकाशित: (2020)