GM1 gangliosidosis type 2

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Name:
GM1 gangliosidosis type 2
Description:
GM1 gangliosidosis type 2 is a clinically variable, infancy or childhood-onset form of GM1 gangliosidosis (see this term) characterized by normal early development and psychomotor regression between seven months and three years of age.
ORPHAcode:
79256
Synonyms:
Juvenile GM1 gangliosidosis
Late-infantile GM1 gangliosidosis
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14