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The Parkinson's Disease was named after James Parkinson. He was a Apothecary also known as a person prepared medicines and sold drugs. Parkinson's Disease is nerve cell damage in the brain causes dopamine levels to drop, leading to the symptoms of Parkinson's.

Parkinson's often starts with a tremor in one hand. Other symptoms are slow movement, stiffness, and loss of balance. This was named in 1817. https://youtu.be/3n8UjH9h_8I

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Reiter's Syndrome

https://youtu.be/DMo8IVBnLWc

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A Lisfranc injury is a eponym names after Jacques Lisfranc , a french man that worked in Napoleon's army as a field surgeon for the soldiers who would get thrown from their horses while riding. When the soldiers got thrown from their horses, their feet would get caught in the stirrupts, which bends the foot a wrong way and dislocates portions of the mid-foot.

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Argyll-Robertson Pupil

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Pupil testing and responses: Argyll Robertson Pupil

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Dissertation - Pupil testing and responses: Argyll Robertson Pupil

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TAY-SACHS DISEASE is name after Warren Tay and Bernard Sachs
https://www.youtube.com/watch?v=CaWoeRY-gJY

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Hashimoto's Disease named after Hakaru Hashimoto
https://www.youtube.com/watch?v=Pi5ou8JRWso

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zollinger-ellison syndrome

https://youtu.be/vAy_KzOv72U

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Anderson Fabry Disease- an inherited disorder that results from the buildup of a particular type of fat, called globotriaosylceramide, in the body's cells.
-also known as Fabry's Disease

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At the Center for Rare Disease Therapy, every child diagnosed with a rare disease receives an individualized treatment plan and family-centered care.

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Alport Syndrome - Named after Arthur Cecil Alport

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Click here to read about Kevin's story: https://alportsyndrome.org/family-stories/kevins-story/ Stay positive. Stay lucky. Stay healthy.

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Colles fracture

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A simple creative powerpoint overview of a colles fracture, or a broken radius. created for my Sports Med. Class. No voice, just video.

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Bogart–Bacall syndrome (BBS) - voice disorder that is caused by abuse or overuse of the vocal cords.( Lauren Bacall )

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Cushing's Disease

https://www.youtube.com/watch?v=OT9nFRmgKWQ

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Still's Disease
https://www.youtube.com/watch?v=dZN-MArjR2M

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Rolando Fracture
a comminuted intra-articular fracture through the base of the first metacarpal bone (the first bone forming the thumb). This is a fracture consisting of 3 distinct fragments; it is typically T- or Y-shaped.
https://youtu.be/NdcSNRS7PRU

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Von Recklinghausen's Disease (Neurofibromatosis)
https://www.youtube.com/watch?v=Tp_9mlJe27E

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Alexander disease by William Stuart Alexander-

1. Alexander disease, also known as fibrinoid leukodystrophy, is a progressive and fatal neurodegenerative disease.

2. https://www.youtube.com/watch?v=rXlFNVmd4AQ

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Aarskog Syndrome
https://www.youtube.com/watch?v=mvlUAvrQYQk

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Wilms Tumor

https://www.youtube.com/watch?v=4S_R80_Mx1Q

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Hodgkin's Disease

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What is Hodgkin Disease? Sign, Symptoms & Causes of Hodgkin Lymphoma

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Subscribe Our YouTube Channel - https://goo.gl/lbSN9U for More Health Info Follow us on Twitter - https://twitter.com/MayoCancerAcdmy View More Info About Cancer awareness - https://goo.gl/sZu2TY Learn About Cancer -- https://goo.gl/BfCKVA If You Think This Video is helpful please Share and Like this & Subscribe Our Channel for Watch More -------------------------------------------------------------------------------------------------------- This video explains Hodgkin's lymphoma.

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Chron's Disease

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Zenker's Diverticulum

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USMLE: What you need to know about Zenker's Diverticulum, by usmleTeam

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I have discussed only important points you need to know for usmle examination, hope it will benefit you thank you SUBSCRIBE NOW: http://bit.ly/161OmbF

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Abels' Test discovered by Dietrich Abels

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Ball's Palsy
https://www.youtube.com/watch?v=V1Wa5eAsp7o

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Harpnup Diesease
https://www.youtube.com/watch?v=HefdunZ1haA

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Addison's disease

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Addison Disease Instructional Tutorial Video

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Enjoy the videos and music you love, upload original content, and share it all with friends, family, and the world on YouTube.

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Lou Gehrig's Disease

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A short documentary about Mike Winston, who is living with Lou Gehrig's disease. More about Mike Winston: http://adf.ly/eLy7G click the button (SKIP AD) on the right above, to see his Facebook site. -- Watch another Video: "A.L.S. Diagnosis": https://youtu.be/YLVywrpDXno --- - What is Amyotrophic lateral sclerosis (ALS): https://youtu.be/Sd7e8CGuge4

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Grave's Disease-Robert James Graves
Autoimmune disease that affects the thyroid.
https://www.youtube.com/watch?v=ySiuqNiVl6s

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Huntington's Disease: Dr. George Huntington diagnosed himself, his father, and his grandfather with this autosomal dominant neurodegenerative disease.

-Breianna Edwards

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Huntington's disease (HD) is a fatal genetic disorder that causes the progressive breakdown of nerve cells in the brain. It deteriorates a person's physical and mental abilities during their prime working years and has no cure. HD is known as the quintessential family disease because every child of a parent with HD has a 50/50 chance of carrying the faulty gene. Today, there are approximately 30,000 symptomatic Americans and more than 200,000 at-risk of inheriting the disease.

Many describe the symptoms of HD as having ALS, Parkinson's and Alzheimer's - simultaneously.

Symptoms usually appear between the ages of 30 to 50, and worsen over a 10 to 25 year period. Ultimately, the weakened individual succumbs to pneumonia, heart failure or other complications. Everyone has the gene that causes HD, but only those that inherit the expansion of the gene will develop HD and perhaps pass it on to each of their children. Every person who inherits the expanded HD gene will eventually develop the disease. Over time, HD affects the individual's ability to reason, walk and speak.

Symptoms Include:

Personality changes, mood swings & depression

Forgetfulness & impaired judgment

Unsteady gait & involuntary movements (chorea)

Slurred speech, difficulty in swallowing & significant weight loss

Stages of HD

Although symptoms of HD vary from person to person, even within the same family, the progression of the disease can be roughly divided into three stages.

Early stage HD usually includes subtle changes in coordination, perhaps some involuntary movements (chorea), difficulty thinking through problems and often a depressed or irritable mood. Medications are often effective in treating depression or other emotional problems. The effects of the disease may make the person less able to work at their customary level and less functional in their regular activities at home.

In the middle stage, the movement disorder may become more of a problem. Medication for chorea may be considered to provide relief from involuntary movements. Occupational and physical therapists may be needed to help maintain control of voluntary movements and to deal with changes in thinking and reasoning abilities. Diminished speech and difficulty swallowing may require help from a speech language pathologist. Ordinary activities will become harder to do.

In the late stage, the person with HD is totally dependent on others for their care. Choking becomes a major concern. Chorea may be severe or it may cease. At this stage, the person with HD can no longer walk and will be unable to speak. However, he or she is generally still able to comprehend language and retains an awareness of family and friends. When a person with HD dies, it is typically from complications of the disease, such as choking or infection and not from the disease itself.

In all stages of HD, weight loss can be an important complication that can correspond with worsening symptoms and should be countered by adjusting the diet and maintaining appetite.

The Scope of HD

Approximately 30,000 Americans have HD, but the devastating effects of the disease touch many more. Within a family, multiple generations may have inherited the disease. Those at-risk may experience tremendous stress from the uncertainty and sense of responsibility. In the community, lack of knowledge about HD may keep friends and neighbors from offering social and emotional support to the family, fostering unnecessary isolation. The Huntington's Disease Society of America has a nationwide network that provides support and referrals for individuals with HD and their families.

HD affects both sexes and all races and ethnic groups around the world.

Who Is At Risk

Every child of a parent with HD has a 50/50 chance of inheriting the expanded gene that causes the disease. If the child has not inherited this expanded gene, he or she will never develop the disease and cannot pass it on to their children.

Genetic Testing & Family Planning

People at-risk for the disease face a difficult choice about genetic testing for HD, given the current absence of an effective treatment or cure. Many people see no benefit in knowing that they will someday develop the disease. Others want an end to uncertainty so that they can make informed choices about the future. The decision whether to test or not is intensely personal and there is no "right" answer.

The Huntington's Disease Society of America recommends that at risk individuals who are considering genetic testing do so at a genetic testing center that follows the HDSA guidelines. Testing procedures at these centers involves sessions with professionals who are knowledgeable about HD and the local services available. It may take several weeks to receive the results once the genetic test is complete.

Genetic testing for children is typically prohibited before the age of 18, as the child may not understand the full implications of testing and may be vulnerable to pressure from others. However, a child under the age of 18 may be tested to confirm a diagnosis of juvenile onset HD after a thorough neurological exam.

Prenatal Testing

For families wishing to have a child who does not have the gene that causes HD, there are a few options. Pre-genetic diagnostic (PGD) testing can be used with In Vitro Fertilization (IVF) to make sure that any fertilized egg implanted does not have the abnormal gene. This can be done without informing the at-risk patient whether or not they have the gene that causes HD. If a woman is already pregnant, she can receive testing for the fetus with a chorionic villus biopsy at 10-11 weeks or via amniocentesis at 14-18 weeks. CLICK HERE TO FIND TESTING CENTERS NEAR YOU.

JHD Overview

In approximately 10% of cases, HD affects children or adolescents. The symptoms of Juvenile HD (JHD) are somewhat different than adult onset HD and may include stiff or awkward walking, increased clumsiness or changes in speech. The ability to learn new information may decline and the child may lose skills they previous had. JHD typically progresses more rapidly than adult onset HD. CLICK HERE FOR MORE INFORMATION

An End To HD?

In 1993, researchers identified the gene that causes HD. Since then, research has moved quickly towards developing treatments and, ultimately, a cure. HDSA supports the goals of clinical and basic research at leading research facilities globally. Clinical and observational trials are an important way you can help to sustain the momentum of HD research and move potential new therapies through the approval process. Visit the Research section of the HDSA website for more information and to find a trial in your area. There are opportunities for all HD family members - gene positive, at-risk, gene negative, and caregivers - to participate.

Where to find help?

With HDSA, no one fights alone. HDSA has developed a nationwide network that includes Chapters, Affiliates, HDSA Centers of Excellence, Support Groups and Social Workers that are ready to assist you with resources in your area.

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Huntington's disease (HD) is a fatal genetic disorder that causes the progressive breakdown of nerve cells in the brain. It deteriorates a person's physical and mental abilities during their prime working years and has no cure. HD is known as the quintessential family disease because every child of a parent with HD has a 50/50 chance of carrying the faulty gene.

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Shinzo Abe

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This transcript has been automatically generated and may not be 100% accurate.

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Video: President Obama Lectured by Japanese Prime Minister Over Okinawa Murder

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That are smokers discussing. I. For a movie lots eight con artist against prison Obama. Seat Japanese prime minister with regard to the most recent case in Okinawa. They'd meet at the decade if it kept my night. I'm when the majority theory. If you don't you'll believe us what you know they had not.

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Eponym- Polio disease
https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=video&cd=3&cad=rja&uact=8&ved=0ahUKEwiw38blhvvOAhXm24MKHXGsAwUQtwIIKDAC&url=https%3A%2F%2Fwww.youtube.com%2Fwatch%3Fv%3D2bWqcZqhr8A&usg=AFQjCNHx7B13aRkIH_978g969FqAwqr5uA

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Hugh Bentall
Created the cardiac surgery that involves a composite graft of the aortic valve, aortic root, and ascending aorta. It's associated with Marfan Syndrome.

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Di Eusanio Marco. Bentall procedure: biological options and  techniques

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Invited lecture at: Heart of Evolution. Innovation in heart valve surgery. May 28-29, 2015. Madrid - Spain

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Carrion's disease
https://www.youtube.com/watch?v=KZ9iYVRmuB0

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Salter-Harris fracture: fractures involving a growth plate
https://www.youtube.com/watch?v=NJXtnDs6mmY

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Down Syndrome
https://www.youtube.com/watch?v=k65kwvFG4sY

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Myocardial Infarction- Heart Attack
https://vimeo.com/110201178

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Riggs disease
https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=1&cad=rja&uact=8&ved=0ahUKEwi44arX_vrOAhXGFx4KHRvHAQkQtwIIHzAA&url=https%3A%2F%2Fwww.youtube.com%2Fwatch%3Fv%3DhKpNwXA7Z4Y&usg=AFQjCNFjQstWFJhDHIKyBqWeW3UZVdB_3A&bvm=bv.131783435,d.amc

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Asperger's Syndrome

https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=video&cd=6&cad=rja&uact=8&ved=0ahUKEwisw4HvhfvOAhUJlx4KHabWC2EQtwIIPTAF&url=https%3A%2F%2Fwww.youtube.com%2Fwatch%3Fv%3DdsC4IsXmXHI&usg=AFQjCNHwLZkiKZJmmkPUa59CanbBnoIZAA&bvm=bv.131783435,d.amc

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Rotor Syndrome
https://www.youtube.com/watch?v=6tNpUVYKouc

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Dr. Bares Award 2013 - 1st Place (Applicant: Ass. Prof. Dr. Mgr. Milan Jirsa, CSc. - Czech Republic)

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Steeg E, Stranecky V, Hartmannova H, Noskova L, Hrebicek M, Wagenaar E, Esch A, Waart R, Elferink RPJO, Kenworthy KE, Sticova E, Edreesi M, Knisely AS, Kmoch S, Jirsa M, Schinkel AH. Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver.

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Alzheimer's Disease
http://nihseniorhealth.gov/alzheimersdisease/symptomsanddiagnosis/video/a3_na.html?intro=yes

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Adams Apple
-The laryngeal prominence (commonly referred to as Adam's apple), a feature of the human neck, is the lump or protrusion that is formed by the angle of the thyroid cartilage surrounding the larynx.

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Quick Questions takes on the matter of the adam's apple -- The fact is, everyone has one! Learn what it really is, what its purpose is, and why they might look different in different people. ---------- Like SciShow? Want to help support us, and also get things to put on your walls, cover your torso and hold your liquids?