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Developmental and epileptic encephalopathy, 55
rareA developmental and epileptic encephalopathy characterized by onset in the first weeks or months of life of refractory seizures, profoundly impaired intellectual development, absent speech, spastic quadriplegia, and dyskinetic movements that has material basis in homozygous or compound heterozygous mutation in the PIGP gene on chromosome 21q22.
- Identifiers
- MONDO:0033364 OMIM:617599
- Causal genes
- PIGP
- Part of
- Disorder of GPI anchor biosynthesisGenetic developmental and epileptic encephalopathyInherited lipid metabolism disorder
- Also known as
- DEE55 · developmental and epileptic encephalopathy 55 · EIEE55 · epileptic encephalopathy, early infantile, 55
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