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1. www.facebook.com › public › Gene-WilsonGene Wilson Profiles | Facebook

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   Gene Wilson. See Photos. View the profiles of people named Gene Wilson. Join Facebook to connect with Gene Wilson and others you may know. Facebook gives people the power to...

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3. www.facebook.com › people › Gene-Wilson-for-DistrictGene Wilson for District 4 Commissioner - Facebook

   www.facebook.com › people › Gene-Wilson-for-District

   Gene Wilson for District 4 Commissioner, Chattanooga Valley, Georgia. 105 likes · 220 talking about this. Political Candidate

4. www.northwestgeorgianews.com › catoosa_walker_newsMeet the Candidates for Walker County Board of Commissioners ...

   www.northwestgeorgianews.com › catoosa_walker_news

   Apr 17, 2024 · Two candidates, both Republicans, are running for the District 4 seat on the Walker County Board of Commissioners: Jamey Hulsey and Gene Wilson. Early voting for the primary elections opens Monday ...

5. ballotpedia.org › Gene_Wilson_(Walker_CountyGene Wilson (Walker County Commissioner Board District 4 ...

   ballotpedia.org › Gene_Wilson_(Walker_County

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   May 21, 2024 · Gene Wilson (Republican Party) is running for election to the Walker County Commissioner Board District 4 in Georgia. Wilson is on the ballot in the Republican primary on May 21, 2024. Jamey Hulsey and Gene Wilson are running in the Republican primary for Walker County Commissioner Board District 4 ...

6. www.ncbi.nlm.nih.gov › books › NBK1512Wilson Disease - GeneReviews® - NCBI Bookshelf

   www.ncbi.nlm.nih.gov › books › NBK1512

   Oct 22, 1999 · Wilson disease is a disorder of copper metabolism that, when untreated, can present with hepatic, neurologic, or psychiatric disturbances – or a combination of these – in individuals ages three years to older than 70 years. Manifestations in untreated individuals vary among and within families.

   • Author: Karl Heinz Weiss, Michael Schilsky

   • Published: 2023/01/12

7. medlineplus.gov › genetics › conditionWilson disease: MedlinePlus Genetics

   medlineplus.gov › genetics › condition

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   Wilson disease is an inherited disorder in which excessive amounts of copper accumulate in the body, particularly in the liver, brain, and eyes. The signs and symptoms of Wilson disease usually first appear between the ages of 6 and 45, but they most often begin during the teenage years. The features of this condition include a combination of ...

8. People also ask

   What is Wilson disease?

   • Wilson disease is an inherited disorder in which excessive amounts of copper accumulate in the body, particularly in the liver, brain, and eyes. The signs and symptoms of Wilson disease usually first appear between the ages of 6 and 45, but they most often begin during the teenage years.

   Wilson disease: MedlinePlus Genetics

   medlineplus.gov/genetics/condition/wilson-disease/

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   Is Wilson disease inherited?

   • Abnormalities in eye movements, such as a restricted ability to gaze upwards, may also occur. Wilson disease is an inherited disorder in which excessive amounts of copper accumulate in the body, particularly in the liver, brain, and eyes. Explore symptoms, inheritance, genetics of this condition.

   Wilson disease: MedlinePlus Genetics

   medlineplus.gov/genetics/condition/wilson-disease/

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   Is Wilson disease autosomal recessive?

   • ED. Wilson disease is inherited in an autosomal recessive manner. Parents of a proband The parents of an affected individual are presumed to be heterozygous for an ATP7B pathogenic variant.

   Wilson Disease - GeneReviews® - NCBI Bookshelf

   www.ncbi.nlm.nih.gov/books/NBK1512/

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   What is the neurologic form of Wilson disease?

   • The neurologic form of Wilson disease has also been known as Westphal-Strumpell pseudosclerosis. The prevalence of Wilson disease is estimated at one in 30,000 in most populations, with a corresponding carrier frequency in the general population of one in 90 [ Sandahl et al 2020 ].

   Wilson Disease - GeneReviews® - NCBI Bookshelf

   www.ncbi.nlm.nih.gov/books/NBK1512/

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9. www.ncbi.nlm.nih.gov › books › NBK441990Wilson Disease - StatPearls - NCBI Bookshelf

   www.ncbi.nlm.nih.gov › books › NBK441990

   Aug 7, 2023 · Wilson disease is an autosomal recessive condition caused by a mutation in the Wilson disease protein (ATP7B) gene. For a person to be affected, a copy of the gene from each parent need to be inherited. Diagnosis is difficult and involves blood tests, urine tests, and a liver biopsy along with the clinical evaluation.