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Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
Am J Med 99:519-524, Haitjema,T.,et al, 1995
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Article Abstract
Thirty-six cases of HHT were found in the 98 persons screened.Pulmonary arteriovenous malformations were found in 12 of the 36 patients(33%),and cerebral arteriovenous malformations in 4(11%).Therapy was recommended in 9 patients with pulmonary arteriovenous malformations and in 2 with cerebral arteriovenous malformations.Family members of known HHT patients should be encouraged to engage in a screening program,since the prevalence of potentially serious locations is higher than previously thought.
 
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familial
genetic neurologic disorders
hereditary hemorrhagic telangiectasia(HHT)
malformation,vascular
malformation,vascular,cerebral
malformation,vascular,familial
malformation,vascular,screening for

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