Ключевые слова: 3d, alpha, autosomal, betahexosaminidase a, brain, cell, chemical, congenital, deficiency, demyelinating, demyelination, disease, disorder, enzyme, gangliosidosis, gene mutation, genetic, gm2, gm2 ganglioside, hexa, hexa gene, hexosaminidase a, human, illustration, infancy, infant, inherited, lamellar, lipid, lysosomal, lysosome, medical, membraneous, metabolic, molecular, myelin, neurology, neuron, neuropathy, ocular, pathology, polypeptide, recessive, science, sphingolipidosis, storage, storage disease, structure, taysachs, tsd,