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:C0042571 (
vertigo
)
7,148
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Eight parameters of blood coagulation and fibrinolysis, i.e., the levels of fibrinogen,
plasminogen
, fibrinogen and/or fibrin-degradation products (FDP), alpha 2-macroglobulin, alpha 1-antitrypsin, CI-inactivator, antiplasmin activity and antithrombin activity, were measured in patients with
vertigo
. Furthermore, the ADP- and collagen-induced platelet aggregations were determined. The results were compared with those for healthy adults. The antiplasmin activity was significantly reduced (p is less than 0.001), the antithrombin activity was significantly reduced (p is less than 0.001) and the platelet aggregation significantly increased (p is less than 0.001), but the levels of fibrinogen,
plasminogen
, FDP, alpha 2-macroglobulin, alpha 1-antitrypsin and CI-inactivator were not significantly altered. The importance of the coagulation-fibrinolysis system and platelet function in patients with
vertigo
is discussed.
...
PMID:Inhibitors of coagulation-fibrinolysis system and platelet function in patients with vertigo. 242 47
We reported a 10-year-old boy with congenital
plasminogen
abnormality resulting in recurrent cerebrovascular ischemic attacks. He suddenly developed dystonia of the left upper limb at 9 years of age. MRI demonstrated small infarcts in the right thalamus and caudate nucleus. He then had a transient ischemic attack at 10 years. He complained of headache,
vertigo
, diplopia, and unsteady gait. DNA analysis revealed that he was heterozygotic for abnormal
plasminogen
. Thus, congenital
plasminogen
abnormality was suspected to be a cause of recurrent cerebrovascular ischemic attacks in this case.
...
PMID:[A case of congenital plasminogen abnormality with recurrent cerebrovascular ischemic attacks]. 1056 90
A 19-year-old Japanese man exhibiting acute right sensorineural hearing loss and
vertigo
was referred to the Jichi Medical School Hospital in June 1994. Although he had no history of recurrent thrombosis and no family history of thrombosis, he had undergone reconstruction of a right foot joint fracture 4 months earlier. Screening studies for
plasminogen
activity demonstrated 10% of normal
plasminogen
activity and his
plasminogen
was diagnosed as "plasminogen Tochigi" by the gene analysis using restriction enzyme Fnu4HI. The patient's hearing returned to normal with administration of heparin, and he was prescribed warfarin for the prevention of thrombosis until October 1995. There was no recurrence of hearing loss during seven years of follow-up. The cause of this patient's hearing loss is believed to be associated with consumption of the already low levels of
plasminogen
as a result of his surgery as well as congenital
plasminogen
disorder.
...
PMID:Acute sensorineural hearing loss and vertigo in a young adult with congenital plasminogen disorder. 1650 59