10 Sep Parálisis supranuclear progresiva. 1. PPAARRÁÁLLIISSIISS SSUUPPRRAANNUUCCLLEEAARR PPRROOGGRREESSIIVVAA DDrraa. La parálisis supranuclear progresiva o síndrome Steele-Richardson-Olszewsky, es una enfermedad rara, degenerativa, producida por el deterioro y muerte. 13 Jan Progressive supranuclear palsy is a neurodegenerative syndrome which was first described in It affects cognition, eye movements and.

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Brain herniation Reye’s Hepatic encephalopathy Toxic encephalopathy Hashimoto’s encephalopathy. Non-drug treatment for PSP can take many forms. Request an Appointment at Mayo Clinic. The cause of PSP is unknown. Poliomyelitis Demyelinating disease Transverse myelitis Tropical spastic paraparesis Epidural abscess. Individuals may suddenly laugh or cry for no apparent reason, they paralisis supranuclear progresiva be apathetic, or they may have paralisis supranuclear progresiva angry outbursts, also for no apparent reason.

In this article arrow-down Diagnosis arrow-down Epidemiology arrow-down Presentation arrow-down Differential diagnosis arrow-down Investigations arrow-down Management arrow-down Complications arrow-down Paralisis supranuclear progresiva. Researchers have found that the deteriorating brain cells of people with progressive supranuclear palsy have abnormal amounts of a protein called tau.

Journal of the Neurological Sciences. Therefore, the H1 haplotype appears to be necessary but not sufficient to cause PSP.

How is PSP different from Parkinson’s disease? Extrapyramidal and movement disorders Cognitive disorders Rare diseases Syndromes. How this process is triggered remains unknown.

In other projects Wikimedia Commons. Whitwell JL, et al. A gastrostomy a minimally invasive surgical procedure prigresiva involves the paralisis supranuclear progresiva of a tube through the skin of the abdomen into the stomach for feeding purposes may be necessary when there are swallowing disturbances or the definite risk of severe choking.

To avoid the hazards of choking, your doctor may recommend a feeding tube. The condition paralisis supranuclear progresiva affects people around the age of 60, and is virtually unknown in people under the age of Patient Platform Limited has used all reasonable care in compiling the paralisis supranuclear progresiva but make no warranty as to its accuracy.

Progressive supranuclear palsy PSP is an uncommon brain disorder that affects movement, control of walking gait and balance, speech, swallowing, vision, mood and behavior, and thinking.

Main anatomical planes and axes applied to suprahuclear sections of the brain. The cause is unknown.

Progressive Supranuclear Palsy Fact Sheet | National Institute of Neurological Disorders and Stroke

Enter Search Term Submit Search. Ann Indian Acad Neurol. This content does not have an Arabic version. This content does not have an English version.

Another possibility is that random genetic mutations, of the kind that occur in all of us all the time, happen to occur in particular cells or certain genes, in just the right combination to injure these cells. Epub Mar If you log out, you will be required to enter your username and password the paralisis supranuclear progresiva time paralisis supranuclear progresiva visit. The symptoms of PSP are caused by a gradual deterioration of brain cells in a few specific areas in the brain, mainly in the region called the brain stem.

Because the symptoms of individuals with PSP progress more rapidly than in other tauopathies, some investigators believe that an anti-tau therapy will show benefit more quickly in PSP clinical trials.

Progressive Supranuclear Palsy

The mission of the National Institute of Neurological Disorders and Stroke NINDS is to seek fundamental knowledge about the brain and nervous system and to use that knowledge to reduce the paralisis supranuclear progresiva of neurological disease. Dementia and Geriatric Cognitive Disorders. Dugger PhD, Joseph G. Progressive supranuclear palsy is the most common atypical Parkinsonian syndrome.

Although healthy individuals also make square-wave jerk movements, PSP patients make slower square-wave jerk movements, with smaller vertical components.

Kim JH, et al. With good attention to medical and nutritional needs, it is possible for individuals with PSP to live a decade or more after the first symptoms of paralisis supranuclear progresiva disease.

Diagnosis Paralisis supranuclear progresiva diagnosis is clinical. Skip to main content.

Progressive supranuclear palsy – Wikipedia

As the disease progresses, most people will begin to develop a blurring of vision and problems controlling eye movement. Epub Nov These complications may include:. Clumps of tau are also characteristic of other neurodegenerative disorders, such as Alzheimer’s disease. Encephalomyelitis Paralisis supranuclear progresiva disseminated Myalgic Meningoencephalitis. On close inspection, eye movements called “square-wave jerks” may be visible paralisis supranuclear progresiva the patient fixes at distance.

By using this site, you agree to the Terms of Use and Privacy Policy. Additional signs and symptoms of progressive supranuclear palsy vary and may mimic those of Parkinson’s disease and dementia.

Progresuva is the paralisis supranuclear progresiva Memory problems and personality changes may also lead a physician to mistake PSP for depression, or even attribute symptoms to some form of dementia. Such imaging markers could be important tools in clinical care to help distinguish PSP from other related disorders, as well as for research to test potential treatments that may not work equally well for outwardly similar disorders.

Other genes, as well as environmental toxinsare being investigated as other possible contributors to the cause of PSP. Approximately six people perpopulation have PSP.

A clinical report on eight cases of ‘heterogeneous system degeneration ‘ paralisis supranuclear progresiva. Excessive eye closing can be treated with botulinum injections.