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Stiff-person syndrome (SPS), also known as stiff-man syndrome, [1] is a rare neurological disorder of unclear cause characterized by progressive muscular rigidity and stiffness. The stiffness primarily affects the truncal muscles and is characterised by spasms , resulting in postural deformities.
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 Idiopathic familial dystonia 333.6 G24.1 Idiopathic nonfamilial dystonia 333.7 G24.2 Spasmodic torticollis: 333.83 G24.3 Idiopathic orofacial dystonia: G24.4 Blepharospasm: 333.81 G24.5 ...
Then, dystonia was reported in detail in 1911, when Hermann Oppenheim, [46] Edward Flatau and Wladyslaw Sterling described some Jewish children affected by a syndrome that was retrospectively considered to represent familial cases of DYT1 dystonia. Some decades later, in 1975, the first international conference on dystonia was held in New York.
Stiff person syndrome is very rare, with only one or two people in a million affected, Johns Hopkins Medicine in Baltimore, Maryland, noted. It affects twice as many women as men, according to the ...
Stiff-person syndrome — often called SPS — is a rare autoimmune disorder, meaning that infection-fighting cells in the body mistakenly attack healthy tissues.
Stiff-person syndrome, aka Moersch-Woltman syndrome, is a neurological disorder that can cause symptoms such as stiffening in the muscles of the trunk, along with stiffness and rigidity in the ...
Stiff person syndrome, which occurs in about one in 1 million people, is characterized by progressive muscle rigidity which leads to impaired mobility, muscle spasms, postural deformities and ...
Stiff-person syndrome; This list is incomplete; you can help by adding missing items. (June 2016) References This page was last edited on 8 September 2024, at 15 ...