Wernicke Encephalopathy and Korsakoff Syndrome Rasheema Douglas School Of New Resources Wernicke Encephalopathy and Korsakoff Syndrome Wernicke Encephalopathy and Korsakoff Syndrome are the acute and chronic stages of the same disease abbreviated as (WKS). (WKS) is a memory brain disorder that can result if there is a very low amount of Vitamin (B1) or Thiamine entering to the brain
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How Genetics Influence Down Syndrome Julia Henry PSY 104 Professor Vincent July 7‚ 2013 How Genetics Influence Down Syndrome Genetics play such an vital role in our development. Every individual carries genes from their mother and their father. Characteristics such as height‚ eye color‚ if we have curly or straight hair are all determined through the our genes and specifically our chromosomes. Many times‚ parents inadvertently pass genes on to their children through their DNA that may contribute
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advantages and disadvantages? Budd Chiari Syndrome •Clinical term used to describe the manifestation of hepatic venous outflow obstruction •Secondary to hepatic vein thrombosis •Or to the narrowing/occlusion of the inferior vena cava (Khan 2009‚Val DC 2003) Ostial stenosis web thrombus Abdominal vein Liver Stomach Gallbladder Enlarged caudate lobe Inferior vena cava Portal vein (Menon et al.‚ 2004) Budd Chiari Syndrome • Primary type -Endoluminal venous (I.e. Thrombosis
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I.Abstract Guillain-Barre Syndrome (GBS) is an auto-immune disease that is rare but can lead to paralysis of limbs and the diaphragm. Ventilatory failure is commonly seen in patients with progressing diseases. The causes of GBS syndrome is unknown‚ however a few culprits are being studied. The most common explanation for GBS is the demyelination of the peripheral nervous system. Other causes in question include flu vaccinations and certain bacteria such as Campylobacter Jejuni. Patients diagnosed
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Asperger syndrome is an autism spectrum disorder and is considered a high functioning form of Autism. Autism spectrum disorders are also known as pervasive developmental disorders and can affect social skills and communication. Asperger syndrome can also delay the development of motor skills and cause sensory problems. While there is no cure for Asperger syndrome‚ there are treatments to help teach the skills affected by Asperger to patients to help them cope with the disorder. Research is currently
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Fetal Alcohol Syndrome Fetal alcohol syndrome is a neurological condition caused by exposure to alcohol during pregnancy. This condition has a lifelong severe effect on the fetus‚ affecting a child’s physical‚ emotional‚ and neurological development. The term fetal alcohol spectrum disorders is used to encompass the range of disabilities associated with exposure to alcohol in utero‚ and includes the diagnosis alcohol-related neurodevelopment disorder (ARND). Signs and symptoms that a child
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information. A click away and I was on my way into Ms. Frizzle of the Magic School Bus’s classroom‚ just waiting to be educated. (Of course‚ there are no Magic School Bus books written about Fragile X‚ my newfound rare genetic disease friend.) Fragile X syndrome affects one in four thousand males‚ and one in every eight thousand females around the globe. Its features include learning disability of varying severity‚ and behavioral problems such as hyperactivity and autistic tendencies. Fragile X’s physical
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Tracie Emmerich Professor Debbie Seale Biology 101 TR‚ 8:30-11:30 am 3/6/2012 Triple X Syndrome Triple X Syndrome is a sex chromosome abnormality in which there are three X chromosomes instead of the usual two found in most females. Triple X Syndrome is also known as Trisomy X‚ Triplo X Syndrome‚ and XXX Syndrome. The first published report of a woman with a karyotype with a 47‚ XXX was by Patricia A. Jacobs in 1959 at a hospital in Scotland. Most people have 46 chromosomes‚ occurring in
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Advocacy for Seniors with Dementia/Alzheimer’s Jeri Fletcher BSHS/441 May 23‚ 2013 Deborah Cujino-Deras Advocacy for Seniors with Dementia/Alzheimer’s Advocacy is defined as a person who advocates on the behalf of an individual or a group. The advocate provides the client support at helping the client resolve issues that affects his or hers daily life (Barsky‚ 2007). Advocating for seniors with Alzheimer’s that face issues with their‚ health and overall wellbeing. This disease threatens
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Andres Schmidt Biology Period- I 05/21/13 Coffin-Lowry Syndrome (CLS) Coffin-Lowy Syndrome Definition: Coffin–Lowry syndrome is a genetic disorder that is X-linked dominant and which causes severe mental problems sometimes associated with abnormalities of growth‚ cardiac abnormalities‚ kyphoscoliosis‚ as well as auditory and visual abnormalities. Grange S. Coffin in 1966 discovered this syndrome‚ in the University of Columbia New York United States of America. Grange S. Coffin Grange
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