Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0018991 (
hemiplegia
)
3,997
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Phosphorus magnetic resonance spectra of resting muscle were obtained from 4 patients with alternating
hemiplegia
of childhood. All patients had abnormally high resonance intensities from inorganic phosphate and an abnormally low calculated cytosolic phosphorylation potential. Two of the 4 patients had abnormally low resonance intensities from phosphocreatine and an abnormally high calculated cytosolic free adenosine diphosphate concentration. These abnormalities are indicative of mitochondrial dysfunction. The combination of a
central nervous system disorder
and evidence of mitochondrial dysfunction in muscle suggests that alternating
hemiplegia
of childhood may represent a previously unrecognized phenotype of mitochondrial disease.
...
PMID:Evidence for mitochondrial dysfunction in patients with alternating hemiplegia of childhood. 849 40
Heterotopic ossification is the formation of new bone in an abnormal location. It is usually seen following
central nervous system disorders
, including spinal cord injury, traumatic brain injury, encephalitis, and burn and trauma. Heterotopic ossification in post-stroke
hemiplegia
is rare; the reported incidence is 0.5-1.2%. It usually occurs on the paretic side of hemiplegic patients. We present here a case of post-stroke
hemiplegia
with heterotopic ossification in the non-paretic limb.
...
PMID:Hemiplegia and heterotopic ossification on the non-paretic extremity: a case report. 1762 86