Neurons in Tay-Sachs disease. Illustration showing swollen neurons with membraneous lamellar inclusions due to accumulation of gangliosides in lysosomes, myelin degradation. Tay-Sachs disease is a disorder that progressively destroys brain neurons, 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.
px | px | dpi | = | cm | x | cm | = | MB |
Details
Creative#:
TPG33142568
Source:
達志影像
Authorization Type:
RF
Release Information:
須由TPG 完整授權
Model Release:
N/A
Property Release:
N/A
Right to Privacy:
No
Same folder images:
anatomicanatomicalanatomyartartworkbrainchildcongenitaldiseaseillustrationinfancyinfantinheritedlysosomalstoragediseasemedicalmedicalillustrationtaysachstay-sachs3d3dimensionalthreedimensionalashkenazijewashkenazijewsjewishchromosome15hexagenehexabeta-HexosaminidaseAtay-sachsdiseaseautosomalrecessivedisordergeneticgm2gangliosidosishexosaminidaseadeficiencylipidstoragelysosomalstoragediseasemetabolicneurologyocularophthalmologyophthalmologypathologyraresphingolipidosisneuronneuronalmoleculemolecularbiochemistrymyelindegradationdegenerationdemyelinationdemyelinating
3153dAaanatomicanatomicalanatomyartartworkashkenaziashkenaziautosomalbeta-Hexosaminidasebiochemistrybrainchildchromosomecongenitaldeficiencydegenerationdegradationdemyelinatingdemyelinationdimensionaldimensionaldiseasediseasediseasediseasedisordergangliosidosisgenegeneticgm2hexahexahexosaminidaseillustrationillustrationinfancyinfantinheritedjewjewishjewslipidlysosomallysosomalmedicalmedicalmetabolicmolecularmoleculemyelinneurologyneuronneuronalocularophthalmologyophthalmologypathologyrarerecessivesachssphingolipidosisstoragestoragestoragetaytay-sachstay-sachsthree