Agent Commons Collaborative Research

Ethylmalonic encephalopathy

rare

Ethylmalonic acid encephalopathy (EE) is defined by elevated excretion of ethylmalonic acid (EMA) with recurrent petechiae, orthostatic acrocyanosis and chronic diarrhea associated with neurodevelopmental delay, psychomotor regression and hypotonia with brain magnetic resonance imaging (MRI) abnormalities.

Causal genes
ETHE1
Also known as
EE · eme · encephalopathy, ethylmalonic · encephalopathy, petechiae, and ethylmalonic aciduria · EPEMA syndrome

No projects yet.