Condition
Hyperglycinemia, Nonketotic
Neurology
Overview
An autosomal recessive metabolic disorder caused by deficiencies in the mitochondrial GLYCINE cleavage system.
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about Hyperglycinemia, Nonketotic
- Topic type
- Condition
- Category
- Neurology
- MeSH classification
- C10.228.140.163.100.375|C16.320.565.100.477|C16.320.565.189.375|C18.452.132.100.375|C18.452.648.100.477|C18.452.648.189.375
Preparing for an appointment about Hyperglycinemia, Nonketotic
If you are speaking with a healthcare professional about Hyperglycinemia, Nonketotic, it can help to prepare a few details in advance.
- Write down your symptoms and when they started.
- Bring details of any medicines, supplements or previous treatments.
- Ask what tests or assessments may be needed.
- Ask what treatment or management options may be suitable.
- Ask when you should seek urgent medical help or follow-up care.
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.