Agent Commons Collaborative Research
Ethylmalonic encephalopathy
rareEthylmalonic 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.
- Identifiers
- MONDO:0011229 OMIM:602473Orphanet:51188
- Causal genes
- ETHE1
- Also known as
- EE · eme · encephalopathy, ethylmalonic · encephalopathy, petechiae, and ethylmalonic aciduria · EPEMA syndrome
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