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GLUT1 deficiency syndrome: E74.810 Attention-deficit hyperactivity disorder (with hyperactivity) 314.01 F90 Tic disorders (involuntary, compulsive, repetitive, stereotyped) F95 Tourette's syndrome: F95.2 Stereotypic movement disorder: F98.5 Huntington's disease (Huntington's chorea) 333.4 G10 Dystonia: G24 Drug induced dystonia: G24.0
Grade I – Low amplitude, rhythmically oscillating joint glide near the resting position of the available arthrokinematic joint play. Activates Type I mechanoreceptors that inhibit nociception and provide information regarding joint position. They have a low threshold and respond to a few grams of tension.
Restless legs syndrome (RLS), (also known as Willis–Ekbom disease (WED), is a neurological disorder, usually chronic, that causes an overwhelming urge to move one's legs. [ 2 ] [ 10 ] There is often an unpleasant feeling in the legs that improves temporarily by moving them. [ 2 ]
Nerve glide, also known as nerve flossing or nerve stretching, is an exercise that stretches nerves. It facilitates the smooth and regular movement of peripheral nerves in the body. It allows the nerve to glide freely along with the movement of the joint and relax the nerve from compression.
Inflammatory demyelinating diseases (IDDs), sometimes called Idiopathic (IIDDs) due to the unknown etiology of some of them, are a heterogenous group of demyelinating diseases - conditions that cause damage to myelin, the protective sheath of nerve fibers - that occur against the background of an acute or chronic inflammatory process.
When accompanied by situs inversus the condition is known as Kartagener syndrome. [ 3 ] Respiratory epithelial motile cilia , which resemble microscopic "hairs" (although structurally and biologically unrelated to hair ), are complex organelles that beat synchronously in the respiratory tract, moving mucus toward the throat.
As hypermobility syndrome can be easily mistaken for being double-jointed or categorised as nothing more than perhaps an achy body from lack of exercise, medical professionals may diagnose those affected incorrectly and not adequately investigate the symptoms. Due to these circumstances many affected individuals can live not knowing they have it.
Remitting seronegative symmetrical synovitis with pitting edema (or sometimes RS 3 PE) is a rare syndrome identified by symmetric polyarthritis, synovitis, acute pitting edema (swelling) of the back of the hands and/or feet, and a negative serum rheumatoid factor. [2]