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Syndromes: Rapid Recognition and Perioperative Implications
) Type II
gangliosidoses; gangliosidoses, gm2.
At a Glance, Synonyms and Classification, Incidence, Genetic Inheritance, Pathophysiology, Diagnosis, Clinical Aspects, Precautions before Anesthesia, Anesthetic Considerations, Pharmacological Implications, Other Conditions to Be Considered, References
Heritable lysosomal storage disorder with ganglioside accumulation leading to severe neurologic impairment with premature death. Tay-Sachs disease (TSD) and its variants are caused by absence or defects of the alpha subunit of hexosaminidase A...."
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