Huntington chorea

Huntington's disease - Symptoms and causes - Mayo Clini

Overview. Huntington's disease is a rare, inherited disease that causes the progressive breakdown (degeneration) of nerve cells in the brain. Huntington's disease has a broad impact on a person's functional abilities and usually results in movement, thinking (cognitive) and psychiatric disorders Huntington Chorea. Huntington's disease (HD) is a genetic disorder in which CAG repeat expansion in the huntingtin gene leads to protein aggregation and death of striatal SPNs (as well as cortical neurons), resulting in chorea, psychiatric problems, cognitive decline, and eventually death What is Huntington's Disease (Chorea)? Huntington's disease causes certain nerve cells in the brain to stop working properly. It leads to mental deterioration and loss of control over major muscle movements. Typically, the symptoms of the illness begin between ages 35 and 50, although they can start as early as childhood or later in life.. Huntington's disease is a hereditary progressive neurodegenerative disorder. One hallmark of the condition is involuntary movements, which include akathisia (restlessness), dystonia (muscle spasms in the arms, head or trunk), and chorea. Chorea is the most common involuntary movement problem in Huntington's disease patients Objective: To develop an evidence-based guideline assessing pharmacologic options for treating Huntington disease (HD) chorea. Methods: We evaluated available evidence from a structured literature review performed through February 2011. Results and recommendations: If HD chorea requires treatment, clinicians should prescribe tetrabenazine (up to 100 mg/day), amantadine (300-400 mg/day), or.

Huntington's disease is a condition that stops parts of the brain working properly over time. It's passed on (inherited) from a person's parents. It gets gradually worse over time and is usually fatal after a period of up to 20 years. Symptoms My mother, 73 years old with Huntington's Chorea. (Watching TV

Huntington Chorea - an overview ScienceDirect Topic

What is Huntington's Disease? Huntington's disease (HD) is a hereditary and deadly disorder that causes nerve cells in the brain tobreak down.This causes physical and mental abilities to weaken. Video of a 38 yr old man with Huntington's disease. Has a strong family history.For more videos: www.neuros.or

Huntington's disease (HD) is an inherited disorder that causes brain cells, called neurons, to die in various areas of the brain, including those that help to control voluntary (intentional) movement. include uncontrolled movements (called chorea), abnormal body postures, and changes in behavior, emotion, judgment, and cognition. People. In this video, I'm going to show & explain to you what Chorea is! Chorea is a symptom of Huntington's disease. It causes involuntary shaking & movement!-----..

Huntington's Disease (Chorea) Guide: Causes, Symptoms and

  1. Huntington's chorea: [ hunt´ing-tunz ] a rare hereditary disease characterized by quick involuntary movements, speech disturbances, and mental deterioration due to degenerative changes in the cerebral cortex and basal ganglia; it appears in adulthood, usually between the ages of 30 and 45, and the patient's condition deteriorates over a period.
  2. Video of a patient with huntington chorea shared with full permission of patient for educational purposes. Notice the movements
  3. ant neurodegenerative disorder characterized by progressive involuntary choreiform movements and cognitive and psychiatric symptoms (Nance, 1998). The disease received widespread recognition after a comprehensive description, On Chorea by George Huntington (1872)

A Huntington-kór (angolul: Huntington's disease, HD) egy neurodegeneratív idegrendszeri betegség, mely az agyban található bizonyos idegsejtek elhalásával jár. Ennek következtében a beteg kezdetben az érzelmi labilitás és a szellemi hanyatlás ( demencia ) később mindezek mellett az akaratlan mozgások ( chorea ) tüneteit mutatja About Press Copyright Contact us Creators Advertise Developers Terms Privacy Policy & Safety How YouTube works Test new features Press Copyright Contact us Creators.

Huntington disease (HD) is an inherited progressive neurodegenerative disorder characterized by choreiform movements, psychiatric problems, and dementia. It is caused by a trinucleotide (cytosine-adenine-guanine [CAG]) expansion in the huntingtin ( HTT) gene on chromosome 4p and inherited in an autosomal-dominant pattern In a survey conducted by the Huntington's Disease Society of America (HDSA) published in 2016, caregivers cited chorea as the most impactful symptom of HD 3,4. As it progresses, movements become more frequent, and appear throughout the body, interfering with activities of daily life. When it does progress, patients become completely dependent.

Huntington's disease is clinically characterized by a triad of motor, cognitive and psychiatric symptoms. Motor features include: impairment of involuntary (chorea) and voluntary movements; reduced manual dexterity, slurred speech, swallowing difficulties, balance problems and falls. It may also present with parkinsonism and dystonia (more. Form Treatment; Huntington's-related: A common treatment is dopaminergic antagonists, although treatment is largely supportive. Tetrabenazine is the only FDA approved drug for the treatment of Huntington's disease-related chorea.: Sydenham's chorea: Haloperidol, carbamazepine and valproic acid.Usually involves antibiotic drugs to treat the infection, followed by drug therapy to prevent recurrence Huntington's chorea is a devastating human genetic disease. A close look at its genetic origins and evolutionary history explains its persistence and points to a potential solution to this population-level problem. People who inherit this genetic disease have an abnormal dominant allele that disrupts the function of their nerve cells, slowly.

Huntington's chorea imposes a direct imprint on the life of the spouse of the affected patient. Interviews with 15 wives of patients with Huntington's chorea revealed that none of them knew prior to marriage of the presence of a heritable disease within the husband's family. When informed of the dia There have been reports that juvenile onset Huntington's chorea is almost always inherited from the father, and that late-onset Huntington's chorea is inherited more often from the mother than from the father. In this larger survey of the parental transmission of disease in Huntington chorea 12 of 1

Chorea in Huntington Disease. Huntington disease (HD) is a hereditary progressive neurodegenerative disorder, in which neurons within the brain break down, resulting in motor, cognitive and psychiatric symptoms. Symptoms generally appear between the ages of 30 to 50 and worsen over a 10 to 25-year period Chorea is a movement disorder that causes involuntary, unpredictable body movements. Chorea symptoms can range from minor movements, such as fidgeting, to severe uncontrolled arm and leg movements Huntingtonova choroba, zkráceně Huntington či HD, dříve známá jako Huntingtonova chorea, je vzácné dědičné neurodegenerativní onemocnění mozku charakteristické nekoordinovanými trhavými pohyby těla a snížením mentálních schopností postihující jedince obojího pohlaví. Dědí se autozomálně dominantně, což znamená, že je přenášeno na normálním chromozomu a. Chorea Huntington: Angehörige, Betroffene und Risikopersonen. Stichwörter. Huntington-Krankheit (HK), Huntingtonsche Erkrankung, Chorea Huntington, Huntingtonsche Chorea, Chorea major, erblicher Veitstanz, großer Veitstanz. Verzeichnis der angebotenen Leistungen. Erfahrungen im Umgang mit dem Thema Chorea Huntington austauschen Huntington disease (HD) is an inherited progressive neurodegenerative disorder characterized by choreiform movements, psychiatric problems, and dementia. It is caused by a cytosine-adenine-guanine (CAG) trinucleotide repeat expansion in the huntingtin ( HTT) gene on chromosome 4p and inherited in an autosomal-dominant pattern

Chorea in Huntington's Disease - Huntington's Disease New

  1. Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia. Prevalence in the Caucasian population is estimated at 1/10,000-1/20,000. Mean age at onset of symptoms is 3
  2. Huntington disease (HD) is an inherited condition that causes progressive degeneration of neurons in the brain. Signs and symptoms usually develop between ages 35 to 44 years and may include uncontrolled movements, loss of intellectual abilities, and various emotional and psychiatric problems
  3. Clinical Worsening and Adverse Events in Patients with Huntington's Disease: AUSTEDO may cause a worsening in mood, cognition, rigidity, and functional capacity. Prescribers should periodically re-evaluate the need for AUSTEDO in their patients by assessing the effect on chorea and possible adverse effects

Huntington's disease (HD) is an autosomal dominantly inherited neurodegenerative disease characterized by progressive motor, behavioral, and cognitive decline, ending in death. Despite the discovery of the underlying genetic mutation more than 20 years ago, treatment remains focused on symptomatic m In 1872, George Huntington wrote a paper on the disease: On Chorea, which is why the disease later became known as 'Huntington's chorea'. Huntington because of the doctor's name, chorea because of the movements. The term is derived from the Greek word 'choreia' which means to dance Definition Huntington's disease (also called Huntington's chorea) is a rare abnormal hereditary disorder of the CNS. It is characterized by chronic progressive chorea (involuntary purposeless, rapid movements) and mental deterioration that results in dementia. Chorea, the Greek word meaning dance. Risk Factors Hereditary (autosomal dominant gene transmission) Idiopathic. Chorea is the most common symptom of Huntington's disease. In the United States, about 4,000 kids a year develop Sydenham chorea after having rheumatic fever . Rheumatic fever is a serious complication of untreated strep throat

in huntington disease This information sheet may help you understand which prescription drugs help treat chorea in people with Huntington disease (HD). Neurologists from the AAN are doctors who identify and treat diseases of the brain and nervous system Huntington disease (HD) is an incurable, adult-onset, autosomal dominant inherited disorder associated with cell loss within a specific subset of neurons in the basal ganglia and cortex. HD is named after George Huntington, the physician who described it as hereditary chorea in 1872 The primary efficacy endpoint was the treatment effect of AUSTEDO vs placebo, as measured by the TMC score, an item of the Unified Huntington's Disease Rating Scale, from baseline to maintenance. On this scale, chorea is rated from 0 to 4 (with 0 representing no chorea) for 7 different parts of the body. The total score ranges from 0 to 28

Huntington disease , also called Huntington chorea, a relatively rare, and invariably fatal, hereditary neurological disease that is characterized by irregular and involuntary movements of the muscles and progressive loss of cognitive ability. The disease was first described by American physician George Huntington in 1872.. Symptoms of Huntington disease usually appear between ages 35 and 50. Huntington's Disease or HD is a progressive or degenerative brain disorder or also known as a Neurodegenerative. Huntington's slowly diminishes the ability think, walk, and talk. Chorea are jerking motions which is a developed symptom of HD. HD slowly ruins the nerves in your brain. As of the science right now Huntingtons is an incurable. Huntington's chorea may also make it difficult to talk, chew, and swallow. 1. In a 2016 survey, care partners reported chorea as the most impactful symptom of Huntington's disease. As Huntington's chorea progresses, people experiencing movements may have pain, and may become increasingly dependent on their care partners for help

Evidence-based guideline: pharmacologic treatment of

Huntington disease (HD) is a progressive disorder of motor, cognitive, and psychiatric disturbances. The mean age of onset is 35 to 44 years, and the median survival time is 15 to 18 years after onset. Full text of GeneReview (by section): Summary Diagnosis Clinical Characteristics Genetically Related (Allelic) Disorders Differential Diagnosis. Hun·ting·ton cho·re·a (hunt'ing-ton), [MIM*143100] a neurodegenerative disorder, with onset usually in the third or fourth decade, characterized by chorea and dementia; pathologically, there is bilateral marked atrophy of the putamen and the head of the caudate nucleus. Autosomal dominant inheritance with complete penetrance, caused by mutation.

huntington chorea for nursing 1. Khai Ho International University of Nursing Professor Geri Mitchell Huntington Running Head: Huntington Chorea Huntingtons sykdom, Huntingtons chorea, setesdalsrykkja eller arvelig sanktveitsdans er en arvelig sjelden sykdom som kjennetegnes av unormale kroppsbevegelser og demens.. Huntingtons sykdom debuterer oftest i 35-50 års alder, sjelden før 20 eller etter 60. Forekomst er i de fleste europeiske folkegrupper anslått til 4-8 per 100 000 the involuntary movements (chorea) of Huntington's disease. AUSTEDO does not cure the cause of the involuntary movements, and it does not treat other symptoms of Huntington's disease, such as problems with thinking or emotions. movements in the face, tongue, or other body parts that cannot be controlled (tardive dyskinesia) Huntington's disease is a genetic disorder.It affects the brain and gets worse over time. This can lead to problems with moving, memory loss as well as thinking skills. Lastly, it also causes changes in behavior. Chorea is one of the main symptoms of Huntington's disease. On average, the disease leads to death about fifteen years after the first signs of the illness show

Huntington's disease - NH

Huntington chorea. 16 likes. Community. My father was a folk song collector, and I grew up listening to the music of Woody Guthrie 57594 On Chorea 1872 George Huntington. Of Pomeroy, Ohio. Essay read before the Meigs and Mason Academy of Medicine at Middleport, Ohio, February 15, 1872. Chorea is essentially a disease of the nervous system. The name chorea is given to the disease on account of the dancing propensities of those who are affected by it, and it is a very. The word chorea is derived from the Latin choreus, meaning dance. Chorea is a hyperkinetic movement disorder characterized by involuntary brief, random, and irregular contractions conveying a feeling of restlessness to the observer [ 1 ]. Chorea may be caused by hereditary neurodegenerative diseases, follow structural damage to deep brain.

Mother Huntington Chorea - YouTub

Enfermedad de Huntington. La enfermedad de Huntington (EH) es un trastorno genético en el cual las neuronas en ciertas partes del cerebro se desgastan o se degeneran. La enfermedad se transmite de padres a hijos Héréditaire, actuellement incurable, la maladie de Huntington est associée à la dégénérescence de neurones d'une partie du cerveau impliqués dans des fonctions motrices, cognitives et comportementales. Si le gène dont l'altération provoque la maladie est connu, les mécanismes qui mènent à cette neurodégénérescence ne sont pas encore élucidés Huntington's Disease Awareness. 501 likes. I made this to page to raise awareness to Huntington's Disease and to help inspire people in all that they do

Huntington's Chorea, also known as Huntington's Disease (HD) was an inherited neurological disease that caused certain nerve cells in the brain to waste away. Those afflicted with the disease were born with the defective gene that was responsible for the disease, although symptoms didn't start appearing until middle age. Early symptoms of the disease may have included uncontrolled movements. The chorea may be severe at this point, causing the affected person to need assistance with all activities of daily living. Ho, Cull, Drake, Barker, Tabrizi, and Lee (2010) conducted a study with 41 participants who had Huntington's disease, concerning voice and quality of life nd genetic choreas, and therapeutic principles are also discussed. Practical clinical points and caveats are included. RECENT FINDINGS C9orf72 disease is the most common Huntington disease phenocopy, according to studies in the European population. Anti-IgLON5 disease can present with chorea. The role of immunotherapies in Sydenham chorea has increased, and further clinical studies may be.

Huntington's Disease: Causes, Symptoms, Treatmen

  1. Chorea Huntington. 942 likes. Raw Punk Berlin. Facebook is showing information to help you better understand the purpose of a Page
  2. ant nedarvning), opkaldt efter den amerikanske læge George Huntington, der beskrev den i 1872.. Sygdommen viser sig først i voksen alder. Ofte er chorea eller sanktvejtsdans et af de tidlige symptomer. I Norge kaldes den ofte setesdalsrykkja.
  3. Huntington's chorea is the result of neuron death in various parts of the brain. Neurons are vital for all aspects of body function. Some neurons (called sensory neurons) transmit information from the sensory organs to the brain. Others (called motor neurons) carry information from the brain and spinal cord to the muscles and glands around the.
  4. Huntington's disease is also sometimes called Huntington's Chorea as the movement appears like a dance (Chorea is the Greek word for dancing.) However chorea is also seen in other.
  5. Huntington's disease is an inherited disease that causes the progressive dying off, or degeneration, of nerve cells in certain parts of the brain. American physician George Huntington wrote the first thorough description of Huntington's disease (HD) in 1872, calling it hereditary chorea to underscore some of its key features
  6. obutyric acid in brain. N Engl J Med. 1973 Feb 15; 288 (7):337-342. [Google Scholar] Bird ED, Iversen LL. Huntington's chorea. Post-mortem measurement of glutamic acid decarboxylase, choline acetyltransferase and dopa
  7. Juvenile Huntington disease (HD) is a less common, early-onset form of Huntington disease that begins in childhood or adolescence. It is a progressive disorder that causes the breakdown of brain cells in certain areas of the brain. This results in uncontrolled movements, loss of intellectual abilities, and emotional disturbances
Chorea Huntington Filmbeitrag - YouTube

Video: Huntington's Disease - YouTub

Huntington's Disease Information Page National Institute

Querschnitt eines gesunden Gehirns (oben) und eines Huntington-Gehirns mit degenerierten Nervenzellen (unten). Stammbaum einer von Chorea Huntington betroffenen Familie. 1.1. Definitionen. plötzliche, schnelle und unregelmäßige Bewegungen verschiedener Muskeln. kann nicht gesteuert werden Huntingtons sykdom er en arvelig sykdom som debuterer i voksen alder og som innebærer svinn av hjerneceller. Det gir seg utslag i typiske ufrivillige og ukontrollerte bevegelser av armer og bein. Huntingtons sykdom er en kronisk sykdom som øker over tid. Forventede leveår etter sykdomsstart anslås til 10 til 25 år. Sist revidert: 11.04.2019 De ziekte van Huntington of Huntingtons chorea (niet te verwarren met de ziekte van Hutchinson) is een ongeneeslijke erfelijke aandoening die bepaalde delen van de hersenen aantast. De eerste symptomen openbaren zich meestal tussen het 35e en 45e levensjaar, maar kunnen ook eerder of later in het leven optreden. De ziekte uit zich onder andere in onwillekeurige (choreatische) bewegingen die.

Huntington's disease (5880985560).jpg 750 × 457; 130 KB Induced Pluripotent Stem Cells of Huntington's Disease.jpg 800 × 249; 29 KB Neuron with mHTT inclusion zoomed.jpg 250 × 205; 76 K Huntington's disease is a complex and severely debilitating disease, for which there is no cure. The most common symptom is jerky movements of the arms and legs, known as 'chorea'. Chorea usually starts as mild twitching and gradually increases over the years

Explaining Chorea Symptoms Huntington's Disease - YouTub

  1. Huntington chorea synonyms, Huntington chorea pronunciation, Huntington chorea translation, English dictionary definition of Huntington chorea. Huntington disease. Translations. English: Hunt·ing·ton dis·ease n. corea; enfermedad de Huntington, padecimiento nervioso que se manifiesta
  2. Chorea Huntington (Huntington- Krankheit) ist auch unter dem Namen Veitstanz geläufig und bezeichnet eine seltene Erbkrankheit, die das Gehirn betrifft und dort Bewegungsstörungen, sowie Wesensveränderungen bis hin zu Demenz bewirkt. Der Ausbruch der Krankheit kann sich in jedem Lebensalter vollziehen, jedoch treten die ersten Symptome.
  3. Deep Brain Stimulation Treatment for Chorea in Huntington's Disease The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government
  4. ant inheritance with complete penetrance, caused by mutation.
  5. Die Huntington-Krankheit ist genetisch bedingt und verursacht Degeneration in bestimmten Hirnbereichen, was zu physischen, mentalen und emotionalen Veränderungen führt. Diese können sich bei jedem Patienten anders auswirken. Einige Merkmale sind Angstzustände, Reizbarkeit, Verfolgungswahn, Psychosen, Demenz, Bewegungs-, Sprach- und.
  6. Speech and voice therapy for Huntington's chorea is best accomplished when aimed at the root of the problem, usually phonation and respiration. Instead of treating the symptom, namely articulation, SLPs will be more likely to meet with success when targeting compensatory strategies for improved respiration and phonation
  7. Die Chorea Huntington wird durch den allmählichen Abbau von Bereichen der Basalganglien, d. h. des Nucleus caudatus und des Putamen, verursacht. Die Basalganglien sind eine Ansammlung von Nervenzellen, die sich in der Hirnbasis, tief im Inneren des Gehirns, befinden. Sie helfen dabei, Bewegungen flüssig zu machen und zu koordinieren
Lesson 2 Huntington’S Chorea

Huntington's chorea definition of Huntington's chorea by

  1. About Chorea in Huntington Disease Huntington disease (HD) is a hereditary progressive neurodegenerative disorder in which neurons within the brain break down, resulting in motor, cognitive and psychiatric symptoms. Symptoms generally appear between the ages of 30 to 50 and worsen over a 10- to 25-year period
  2. Huntington's chorea: investigation into the prevalence of this disease in the area covered by the North East Metropolitan Regional Hospital Board. Brain 1967; 90 (1): 203 -32.CrossRef Google Scholar PubMe
  3. ation brain dementia electroencephalography (EEG) epilepsy genes genetics microscopy neurochemistry neuropathology occupational therapy personality Authors and affiliation
  4. Chorea is a primary feature of Huntington's disease, a progressive, hereditary movement disorder that appears in adults, but it may also occur in a variety of other conditions. Syndenham's chorea occurs in a small percentage (20 percent) of children and adolescents as a complication of rheumatic fever

(1994) A comparison of the regularity of involuntary muscle contractions in vascular chorea with that in Huntington's chorea, hemiballism and parkinsonian tremor Chorea is a movement disorder that causes involuntary, unpredictable body movements. Chorea symptoms can range from minor movements, such as fidgeting, to severe uncontrolled arm and leg movements Huntington's Disease Support Center. Welcome to our Huntington's Disease Support Center! Here you are welcome to discuss any issue related to Huntington's disease. You must be registered to participate. Check the guidelines for more information. Thanks for visiting. Page 1 of 304 Pages: 12 3 4 5. Forums New Huntington's chorea definition, a hereditary disease of the central nervous system characterized by brain deterioration and loss of control over voluntary movements, the symptoms usually appearing in the fourth decade of life. See more Die Erkrankung Huntington s Chorea ist eine autosomal dominant vererbte Erkrankung, die gewöhnlich im mittleren Lebensabschnitt beginnt und unausweichlich zum Tode führt. In unserem Bestreben, Proteine zu identifizieren, welche an Prozessen Upstream oder Downstream des krankheitsverursachenden Proteins Huntingtin beteiligt sind, wurde das.

Huntington Chorea - YouTub

Huntington's chorea translate: (同 Huntington's disease). Learn more in the Cambridge English-Chinese traditional Dictionary Huntington's chorea definition: a rare hereditary type of chorea , marked by involuntary jerky movements, impaired... | Meaning, pronunciation, translations and example

Neurology - Topic 17 Huntingtons disease - patient - YouTube

Symptoms of Huntington's disease most often appear around 30 to 40 years of age. Early signs and symptoms may include irritability, depression, small involuntary movements, poor coordination, and cognitive impairment. Many develop involuntary jerking or twitching movements called chorea which becomes more pronounced as the disease progresses Chorea Huntington Dissertation, how to begin to write an descriptive essay, dissertation defense academia, hammurabi research paper. College. July. Follow us. AU: Revisions. for $20.90 Free. Students Reviews. Finance. 0%. 100% Daily Orders. 100% » Chemical Engineering » Civil Engineering. Chorea is a type of dyskinesia characterized by sudden, rapid, involuntary, and purposeless movements that happen during a person's normal voluntary movement.. Pathology. It is a clinical symptom related to different etiologies, such as infectious, inflammatory, vascular, hereditary (e.g. Huntington's disease), drug-induced, degenerative, and neoplastic causes 1,2

Drugs used in essential tremor, chorea, tics, and related disorders. Tetrabenazine is mainly used to control movement disorders in Huntington's chorea and related disorders. Tetrabenazine can also be prescribed for the treatment of tardive dyskinesia if switching or withdrawing the causative antipsychotic drug is not effective. It acts by depleting nerve endings of dopamine Huntington's disease (HD), which results from an abnormal polyglutamine extension in the N-terminal region of the huntingtin protein, the gene for HD, is an autosomal dominant neurodegenerative disorder characterized by motor, behavioral, and cognitive dysfunction ().HD is one of several genetic syndromes sometimes associated with diabetes (), although there is inconsistency among the reports. Efficacy, Safety, and Tolerability of Valbenazine for the Treatment of Chorea Associated With Huntington Disease (KINECT-HD) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government For chorea severity, physicians were asked to either provide Unified Huntington's Disease Rating Scale (UHDRS) scores or to rate chorea severity (mild, moderate, or severe). Treatment history data in patients using tetrabenazine included the initial dose, duration of the titration period, maintenance dose, dosage changes, reason for dosage. La maladie de Huntington (parfois appelée chorée de Huntington) est une maladie héréditaire et rare, qui se traduit par une dégénérescence neurologique provoquant d'importants troubles moteurs, cognitifs et psychiatriques, et évoluant jusqu'à la perte d'autonomie puis la mort [1].Plusieurs pistes de traitements sont en cours d'expérimentation

File:Huntington Disease patient and control MRIDaniel My Brother (Huntington's Disease) - YouTubeChorea Huntington Betreuung - Schloss HausWhat It's Like To Be In A Family Cursed With Huntington's