warfarin has been researched along with Noonan-Syndrome* in 2 studies
2 other study(ies) available for warfarin and Noonan-Syndrome
Article | Year |
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Warfarin-induced impairment of bone material quality in a patient undergoing maintenance hemodialysis: A case report.
The use of warfarin in patients undergoing hemodialysis is associated with decreased bone mineral density and an increased incidence of bone fracture. However, no studies to date have directly estimated bone quality with bone histomorphometry in patients with bone abnormalities who are taking warfarin and undergoing hemodialysis.. A 47-year-old female with Noonan syndrome presented with progressive bilateral lower extremity pain on walking, and skin sclerosis. She had been undergoing maintenance hemodialysis for 25 years following 2 years of peritoneal dialysis for chronic glomerulonephritis. She had been taking warfarin as an anticoagulant agent for 13 years after she underwent an aortic valve replacement.. Warfarin-induced impairment of bone material quality.. Histomorphometric analysis of the bone biopsy specimens showed impairment in bone calcification processes, a high turnover of bone remodeling, low bone volume, and mild fibrosis. The bone abnormality could not be categorized into any type of representative bone disease classification such as osteitis fibrosa, osteomalacia, adynamic bone disease, uremic osteodystrophy, or hyperparathyroidism, but was consistent with warfarin-induced impairment of bone material quality.. Warfarin can induce impairment of bone material quality in a patient undergoing hemodialysis. Topics: Anticoagulants; Bone Density; Chronic Kidney Disease-Mineral and Bone Disorder; Female; Humans; Middle Aged; Noonan Syndrome; Renal Dialysis; Warfarin | 2020 |
Noonan syndrome and moyamoya.
We report a patient with Noonan syndrome and asymptomatic cardiac disease (supravalvular aortic stenosis and pulmonary valvular stenosis) who had frequent transient ischemic attacks. Bilateral moyamoya was evident; in addition, he manifested activated protein C resistance and was heterozygous for the factor V Leiden mutation. Anticoagulation abolished his episodes and, despite extensive cerebrovascular disease, he has no permanent neurologic deficits. The association between Noonan syndrome and moyamoya has not previously been described. Disruption of vascular development in prenatal life may have resulted in both cardiac and cerebrovascular disease in this child. Topics: Anticoagulants; Cerebral Angiography; Child; Drug Resistance; Humans; Ischemic Attack, Transient; Male; Moyamoya Disease; Noonan Syndrome; Protein C; Warfarin | 1997 |