例句與造句

1. Children with infantile neuroaxonal dystrophy experience progressive difficulties with movement.
2. Other rare disorders, such as various neuroaxonal dystrophies, also have ?-synuclein pathologies.
3. Mutations in the " PLA2G6 " gene have been identified in most individuals with infantile neuroaxonal dystrophy.
4. A few individuals with infantile neuroaxonal dystrophy have not been found to have mutations in the " PLA2G6 " gene.
5. In some individuals with infantile neuroaxonal dystrophy, abnormal amounts of iron accumulate in a specific region of the brain called the basal ganglia.
6. It's difficult to find neuroaxonal dystrophy in a sentence. 用neuroaxonal dystrophy造句挺難的
7. A new neurodegenerative disorder, called " Neuroaxonal Dystrophy ", that was originally identified in Spanish Water Dogs has been identified in the breed in 2016.
8. Other diseases in the differential diagnosis of adult-onset DRPLA include Unverricht-Lundborg, Neuroaxonal dystrophy, Gaucher's disease, Sialidosis, and Galactosialidosis.
9. Additional neurological and neuromuscular symptoms such as diminished muscle tone, weakness, involuntary rapid eye movements, neuroaxonal dystrophy from birth, discoloration of skin, Telangiectasia or widening of blood vessels.
10. Infantile neuroaxonal dystrophy is characterized by the development of swellings called spheroid bodies in the axons, the fibers that extend from nerve cells ( neurons ) and transmit impulses to muscles and other neurons.
11. Rapid, involuntary eye movements ( nystagmus ), eyes that do not look in the same direction ( strabismus ), and vision loss due to deterioration ( atrophy ) of the optic nerve are characteristic of infantile neuroaxonal dystrophy.
12. Although it is unknown how changes in this enzyme's function lead to the signs and symptoms of infantile neuroaxonal dystrophy, phospholipid metabolism problems have been seen in both this disorder and a related disorder called pantothenate kinase-associated neurodegeneration.
13. Researchers are studying the links between phospholipid defects, brain iron, and damage to nerve cells, but have not determined how the iron accumulation that occurs in some individuals with infantile neuroaxonal dystrophy may contribute to the features of this disorder.