C1–C2 Disc Derangement
Before reading RX Patient Tools Use these quick guides before reading the article, or return to them when you need help preparing questions for a doctor....
Browse medical articles by letter, category, and search. Built for large health libraries.
Before reading RX Patient Tools Use these quick guides before reading the article, or return to them when you need help preparing questions for a doctor....
DefinitionC1–C2 discogenic pain? syndrome is neck pain? arising directly from degenerative or injurious changes in the intervertebral disc between the first (atlas) and second (axis) cervical?...
DefinitionC1–C2 facet joint arthritis?, also known as atlantoaxial facet arthropathy, is a degenerative condition affecting the small synovial joints that connect the first cervical? vertebra (atlas)...
DefinitionC1–C2 facet joint arthropathy is a form of osteoarthritis? affecting the small, paired synovial joints between the first (atlas) and second (axis) cervical? vertebrae. Over time,...
DefinitionC1–C2 facet joint osteoarthritis? is a degenerative condition affecting the uppermost joints of the spine, located between the first cervical? vertebra (atlas) and the second cervical...
DefinitionInternal disc disruption (IDD) at the C1–C2 level refers to microscopic tears and degeneration within the nucleus pulposus and inner annulus fibrosus of the atlantoaxial disc....
DefinitionNucleus pulposus dehydration? refers to the loss of water content and glycosaminoglycan matrix within the gelatinous core of an intervertebral disc. In the atlas–axis complex (C1–C2),...
DefinitionA C1–C2 spine sprain?, often called an atlantoaxial ligament? sprain?, occurs when one or more ligaments connecting the first cervical? vertebra (atlas) and the second cervical...
DefinitionC11orf73-related autosomal recessive hypomyelinating leukodystrophy is a rare brain white-matter disease that starts in infancy. In this condition, the fatty insulation (myelin) around nerve fibers in...
DefinitionC11ORF73-related autosomal recessive hypomyelinating leukoencephalopathy is a rare genetic brain white-matter disease. “Hypomyelinating” means the brain does not lay down normal myelin (the fatty insulation around...
DefinitionC12orf65 combined oxidative phosphorylation deficiency is a very rare genetic disease that affects how the “power stations” of the cell (mitochondria) make energy. In this condition,...
DefinitionC1q deficiency is a very rare inherited immune problem where the body makes too little—or none—of a protein called C1q. C1q is the “starter” of the...