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Type 1 gm1 gangliosidosis

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Type 1 GM1 gangliosidosis --> infantile generalised GM1 gangliosidosis

One of the hereditary metabolic diseases of infancy; resembles tay-Sachs disease, except other organ systems (bone, liver, kidney) are affected.

Synonym: familial neuroviscerolipidosis, pseudo-Hurler disease, type 1 GM1 gangliosidosis.