Tay-Sachs disease, a lysosomal storage genetic disorder, 3D illustration. A child with macrocephaly, and close-up view of swollen neurons with lamellar inclusions due to accumulation of gangliosides
Tags
3d ashkenazi autosomal baby beta-hexosaminidase a brain child chromosome 15 congenital deficiency demyelination diagram disease disorder dna enlarged enzyme ganglioside gangliosidosis gene gene mutation genetic gm2 gm2 ganglioside hexa hexa gene hexosaminidase a illustration infant inherited jew lipid lysosomal lysosome macrocephaly metabolic metabolism molecule mutation neurology neuron polypeptide recessive retina sphingolipidosis storage storage disease tay-sachs tsd
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License and Use
Free for commercial use No attribution required
- Created With Redmond.ai
- Details
- Published on Nov 09, 2022
- Photo type JPG
- Category Science