Tay-Sachs disease, illustration. A genetic disorder that progressively destroys brain neurons. It is caused by a mutation in the HEXA gene of chromosome 15 leading to deficiency of hexosaminidase A. Tay-sachs is most commonly seen in infants, manifesting in muscle weakness and decreased motor function, vision and hearing loss, and intellectual disability.
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TPG33142536
Source:
達志影像
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RF
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須由TPG 完整授權
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N/A
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anatomicanatomicalanatomyartartworkbrainchildcongenitaldiseaseillustrationinfancyinfantinheritedlysosomalstoragediseasemedicalmedicalillustrationtaysachstay-sachs3d3dimensionalthreedimensionalashkenazijewashkenazijewsjewishchromosome15hexagenehexabeta-HexosaminidaseAtay-sachsdiseaseautosomalrecessivedisordergeneticgm2gangliosidosishexosaminidaseadeficiencylipidstoragelysosomalstoragediseasemetabolicneurologyocularophthalmologyophthalmologypathologyraresphingolipidosisneuronneuronalmoleculemolecularbiochemistrydna
3153dAaanatomicanatomicalanatomyartartworkashkenaziashkenaziautosomalbeta-Hexosaminidasebiochemistrybrainchildchromosomecongenitaldeficiencydimensionaldimensionaldiseasediseasediseasediseasedisorderdnagangliosidosisgenegeneticgm2hexahexahexosaminidaseillustrationillustrationinfancyinfantinheritedjewjewishjewslipidlysosomallysosomalmedicalmedicalmetabolicmolecularmoleculeneurologyneuronneuronalocularophthalmologyophthalmologypathologyrarerecessivesachssphingolipidosisstoragestoragestoragetaytay-sachstay-sachsthree
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