Parkinson's Diseases Specialist Redford MI

In the more likely scenario, having only one copy of the mutation increases the risk of the disease, but the disease will only express itself in the presence of other genetic or environmental factors.

Andrew L Marcus MD
(313) 730-9100
3815 Pelham St
Dearborn, MI
Specialties
Neurology

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Hermann Darwin Banks, MD
Detroit, MI
Specialties
Neurology
Gender
Male
Education
Medical School: Wayne State Univ Sch Of Med, Detroit Mi 48201
Graduation Year: 1994

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Richard Donald Fessler, MD
(248) 784-3667
29275 Northwestern Hwy Ste 100
Southfield, MI
Specialties
Neurological Surgery, Vascular & Interventional Radiology
Gender
Male
Education
Medical School: Univ Of Mi Med Sch, Ann Arbor Mi 48109
Graduation Year: 1987
Hospital
Hospital: St Mary Hospital, Livonia, Mi; Harper Hospital, Detroit, Mi
Group Practice: University Neurosurgical Assoc

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Lalit Chamanlal Parekh, MD
(586) 427-1000
Southfield, MI
Specialties
Neurology
Gender
Male
Education
Medical School: Bj Med Coll, Gujarat Univ, Ahmedabad, Gujarat, India
Graduation Year: 1967

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Veronica Sosa, MD
(313) 916-2600
Southfield, MI
Specialties
Neurology
Gender
Female
Education
Medical School: Univ Of Ct Sch Of Med, Farmington Ct 06032
Graduation Year: 1992
Hospital
Hospital: Henry Ford Hospital, Detroit, Mi
Group Practice: Henry Ford Medical Center Pierson; Henry Ford Medical Group

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Kevin R Lee MD
(248) 926-4292
136 S Pontiac Trl
Walled Lake, MI
Specialties
Neurology

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Richard M Trosch
(248) 355-3875
26400 W 12 Mile Rd
Southfield, MI
Specialty
Neurology

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Henry D Messer, MD FACS
23248 Bonair St
Dearborn Heights, MI
Gender
Male
Education
Medical School: Duke
Graduation Year: 1950

Data Provided by:
Brian Nolan Kirschner
(248) 355-3875
26400 W 12 Mile Rd
Southfield, MI
Specialty
Neurology

Data Provided by:
Mark Goldberger
(248) 784-3708
29275 Northwestern Hwy
Southfield, MI
Specialty
Neurosurgery

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Another Genetic Risk for Parkinson's

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By Kathryn Ayers

A number of small studies have suggested that a mutation in the gene that produces the protein alpha-synuclein (SNCA) may play a role in the onset of the degenerative neurological condition known as Parkinson’s disease. Now a large multi-nation study confirms that the mutation can increase the risk of Parkinson’s by 50 percent. Researchers at the Mayo Clinic sifted data on some 2,700 Parkinson’s patients and an equal number of age- and sex-matched healthy individuals and determined that “the SNCA gene is not only a rare cause of autosomal dominant Parkinson’s disease in some families, but also a susceptibility gene for Parkinson’s disease at the population level.” People who have the misfortune of inheriting copies of the gene mutation from both parents—a rare occurrence—will contract Parkinson’s. In the more likely scenario, having only one copy of the mutation increases the risk of the disease, but the disease will only express itself in the presence of other genetic or environmental factors. The researchers estimate that the SNCA gene accounts for roughly 3 percent of all Parkinson’s cases—about the same, they say, “as the population effect of other common variants implicated in Parkinson’s disease.”

Author: Kathryn Ayers

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