···
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. Image details File size:
100.3 MB (1.5 MB Compressed download)
Open your image file to the full size using image processing software.
Dimensions:
5920 x 5920 px | 50.1 x 50.1 cm | 19.7 x 19.7 inches | 300dpi
Search stock photos by tags
Similar stock images RF 2HBA1EF – Neurons in Tay-Sachs disease. Illustration showing swollen neurons with membraneous lamellar inclusions due to accumulation of gangliosides in lysosomes. 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. RF 2HBA1DY – Neurons in Tay-Sachs disease. Illustration showing swollen neurons with membraneous lamellar inclusions due to accumulation of gangliosides in lysosomes. 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. RF 2HBA1E7 – 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. RF 2HBA1E6 – 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. RF 2HBA1FH – 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. RF 2HBA1DP – 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. RF 2HBA1D6 – 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. RF 2HBA1EN – Neurons in Tay-Sachs disease. Illustration showing swollen neurons with membraneous lamellar inclusions due to accumulation of gangliosides in lysosomes. 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. RF 2HBA1EK – Neurons in Tay-Sachs disease. Illustration showing swollen neurons with membraneous lamellar inclusions due to accumulation of gangliosides in lysosomes. 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. RF 2HBA1E9 – Neurons in Tay-Sachs disease. Illustration showing swollen neurons with membraneous lamellar inclusions due to accumulation of gangliosides in lysosomes. 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. RF 2HBA1E0 – Neurons in Tay-Sachs disease. Illustration showing swollen neurons with membraneous lamellar inclusions due to accumulation of gangliosides in lysosomes. 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. RF 2HBA1EW – Neurons in Tay-Sachs disease. Illustration showing swollen neurons with membraneous lamellar inclusions due to accumulation of gangliosides in lysosomes. 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.