Property:Has condition classification

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Showing 20 pages using this property.
C
CRPS I, CRPS II  +
Formative, resting, and resorptive stages.  +
CESS (cauda equina suspected), CESI (cauda equina incomplete), CESR (cauda equina with urinary retention).  +
Typical and atypical phenotypes  +
Phenotypic spectrum ranging from severe Ullrich congenital muscular dystrophy (UCMD) with early-onset weakness and contractures, to milder Bethlem myopathy with later onset and slower progression.  +
Non-cardiac musculoskeletal chest pain syndrome; distinguished from Tietze syndrome by absence of swelling.  +
D
Niwayama and Utsinger, and Resnick for research purposes  +
Nodules, cords, contractures  +
F
CAM, Pincer, or mixed  +
Can be primary or secondary to another pain condition.  +
H
HNPP is classified under hereditary demyelinating neuropathies and distinct from other polyneuropathies due to its episodic nature.  +
Primary and secondary  +
I
Infantile, Juvenile, Adolescent, Adult.  +
Belong to the trigeminal autonomic cephalalgias.  +
Proximal and distal forms.  +
Extra-articular hip impingement condition.  +
P
Pompe disease presents in two forms: infantile-onset, characterized by hypertrophic cardiomyopathy and hypotonia, and late-onset, characterized by limb girdle and axial weakness and respiratory insufficiency in late disease.  +
S
Type I: rigid thoracic hyperkyphosis Type II: lumbar disease  +
Length-dependent, non-length dependent, or mono-multiplex neuropathy types based on symptom distribution.  +
T
Neurogenic (NTOS), Arterial (ATOS), Venous (VTOS)  +