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Screening for von Hippel-Lindau Disease by DNA Polymorphism Analysis
JAMA 267:1226-1231, Glenn,G.M.,et al, 1992
See this aricle in Pubmed

Article Abstract
DNA polymorphism analysis predicted nine disease gene carriers and 33 individuals with the wild-type(normal)allele among the 48 individuals at risk of developing VHL disease;the test was not informative in six individuals.All nine individuals predicted to carry the VHL gene had evidence of occult disease on clinical examination.There was no clinical evidence of VHL disease in 32 of 33 individuals predicted to carry the wild-type allele.DNA polymorphism analysis can identify individuals likely to carry the VHL disease gene among asymptomatic members of disease families.This technique serves to focus attention on those individuals who require periodic medical examination and may help to alleviate the morbidity and mortality associated with this disease.
 
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DNA probes
gene
genetic linkage
genetic neurologic disorders
genetic screening
molecular genetics
RFLPs
Von Hippel Lindau
Von Hippel Lindau,carrier
Von Hippel Lindau,screening protocol for

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