Atypical glycine encephalopathy

MONDO:0015010

Atypical glycine encephalopathy is a rare form of glycine encephalopathy (GE) presenting disease onset or clinical manifestations that differ from neonatal or infantile GE.

Also known as: atypical NKA, atypical non-ketotic hyperglycinemia, GLYCINE encephalopathy with normal serum GLYCINE, Glycine encephalopathy with normal serum Glycine

26 clinical trials for this condition and its sub-types.

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