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GM1 gangliosidosis type 2
rareGM1 gangliosidosis type 2 is a clinically variable, infancy or childhood-onset form of GM1 gangliosidosis characterized by normal early development and psychomotor regression between seven months and three years of age.
- Identifiers
- MONDO:0009261 OMIM:230600Orphanet:79256
- Part of
- GM1 gangliosidosis
- Also known as
- gangliosidosis generalised GM1 juvenile type · gangliosidosis generalised GM1 type 2 · gangliosidosis generalized GM1 juvenile type · gangliosidosis generalized GM1 type 2 · gangliosidosis, generalised GM1, juvenile type
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