What is Asperger's Syndrome?
Autism Society of America: Autism FAQWhat distinguishes Asperger's Syndrome from autism is the severity of the symptoms and the absence of language delays. Children with Asperger's may be only mildly affected and frequently have good language and cognitive skills. To the untrained observer, a child with Asperger's may seem just like a normal child behaving differently. They may be socially awkward, not understanding of conventional social rules, or show a lack of empathy.
Related QuestionsWhat is an epileptic syndrome?
UC Davis Comprehensive Epilepsy Program - FAQ about epilepsyUntil recently, neurologists classified the types of seizures, such as focal or generalized convulsive. The past few decades, research has leaned toward determining if the patient has an epileptic syndrome, or a specific type occurring under certain conditions. These conditions could include a particular clinical setting at a certain age with other accompanying findings like radiological tests and EEGs. Absence--or petit mal--seizures can illustrate the value of a syndrome approach.
Related QuestionsWhat is a Syndrome?
CdLS USA Foundation: Facts About CdLSSyndrome" is a medical term for a condition in which there is a collection of signs (observable body changes) and symptoms (problems observed by the patient) recognizable by a doctor's exam. Individuals with a syndrome may not have all of its associated signs and symptoms, but they must have enough to be considered "diagnostic." Conversely, because someone may display some of the signs and symptoms of a syndrome, does not necessarily mean they have it.
Related QuestionsWhat is HELLP Syndrome?
Preeclampsia FAQHELLP Syndrome occurs in 4 percent to 12 percent of the women who have preeclampsia. It is one of the most severe forms of preeclampsia. HELLP stands for: hemolysis, elevated liver enzymes, and lowered platelets. HELLP Syndrome most often affects the liver, causing stomach and right shoulder pain. HELLP Syndrome is most dangerous because it can occur before you exhibit the classic symptoms of preeclampsia. It is often mistaken for the flu or gallbladder problems.
Related QuestionsIs Down syndrome inherited?
Down Syndrome: FAQOnly 3 to 5% of cases are inherited; the rest arise as an accident of chromosome arrangement during meiosis. For details, see my essay on the origin of trisomy 21 or Dr. Paul Benke's essay on the types of DS, and the risk and recurrence risk of DS. No. Down syndrome occurs at conception, so nothing in the pregnancy can cause Down syndrome to occur. As for prior to conception, the research all shows that drug or alcohol use does not increase the risk of having a child with DS.
Related QuestionsWhat is Tourette Syndrome?
Tourette Syndrome FAQTourette Syndrome TS) is a neurological disorder characterized by tics -- involuntary, rapid, sudden movements or vocalizations that occur repeatedly in the same way.
Related QuestionsBlog For Down Syndrome & FAQ About Down SyndromeDown syndrome is a chromosomal disorder that includes some degree of mental retardation, as well as a combination of birth defects, including neurologic impairment, characteristic facial features and, often, heart defects and visual and hearing impairment. The severity of all these problems varies greatly among affected individuals. Down syndrome is one of the most common genetic birth defects, affecting approximately one in 800 to 1,000 babies.Related Questions
What is Down's Syndrome?
FAQDown's Syndrome is a genetic condition caused by extra genetic material (genes) from the 21st chromosome. The extra genes cause certain characteristics that we know as Down's syndrome. Individuals with Down's Syndrome also have all the other genes given to them by their parents. As a result, they have a combination of features typical of Down's Syndrome on top of the individual features from their parents.
Related QuestionsUC Davis Children's Hospital: Child Neurology Clinic ?- freq...Down syndrome is the most prominent cause of birth defects. It also is known as “Trisomy 21” because Down syndrome is the most prominent cause of birth defects. It also is known as “Trisomy 21” because it results from an abnormality of the 21st chromosome. Down syndrome typically affects facial appearance, height and size and shape of the hands, and also can produce abnormalities of the heart and digestive system that may require corrective surgery.Related Questions
MUSC Children's Hospital - Down Syndrome CenterDown syndrome is a genetic disorder that includes a combination of birth defects, including some degree of mental retardation, characteristic facial features and, often, heart defects, visual and hearing impairment, and other health problems. The severity of all of these problems varies greatly among affected individuals. Down syndrome is one of the most common genetic birth defects, affecting approximately one in 800 to 1,000 babies.Related Questions
WHAT IS THE LONG QT SYNDROME (LQTS)?
QTsyndrome.ch - Frequently Asked Questions (FAQ)The long QT syndrome (LQTS) is causing an abnormality of the heart's electrical system. The mechanical function of the heart is entirely normal. The electrical problem is due to defects in heart muscle cell structures called ion channels. These electrical defects predispose affected persons to a very fast heart rhythm (arrhythmia) called "Torsade de Pointes" (TdP) which leads to sudden loss of consciousness (syncope) and may cause sudden cardiac death.
Related QuestionsHOW IS LONG QT SYNDROME DIAGNOSED?
QTsyndrome.ch - Frequently Asked Questions (FAQ)The diagnosis is commonly suspected or made from the electrocardiogram (ECG). All children and young adults should have an ECG as part of their evaluation for an unexplained loss of consciousness episode. On the other hand, there is the possibility to check blood samples for known gene mutations that cause LQTS.
Related QuestionsI might have carpal tunnel syndrome. Should I see a Chiropractor?
Chiropractic Care, Acupuncture, & Massage Therapy. Austi...Carpal tunnel syndrome (CTS) usually begins with occasional hand and wrist numbness. Most people ignore CTS when it is in its early stages. Over time, the numbness persists and turns into pain and hand weakness. People at risk for CTS include computer operators and anyone who performs a repetitive hand motion frequently. Early detection and treatment is important. Since different people have different pain thresholds, it's best to be screened by a trained professional.
Related QuestionsWhat is Lowe syndrome?
Frequently Asked QuestionsLowe syndrome (LS) is a rare genetic condition affecting males that causes physical and mental handicaps and medical problems. Also called the oculo-cerebro-renal syndrome of Lowe (OCRL), it was first described in 1952 by Dr. Charles Lowe and colleagues.
Related QuestionsWhat is Poland's Syndrome?
FAQ Frequently Asked Questions about Poland's Syndrome at ww...Poland syndrome is a unique pattern of one-sided malformations that are present at birth. Poland syndrome is characterized by a defect of the chest (pectoralis) muscle on one side of the body and webbing of the fingers (cutaneous syndactyly) of the hand on the same side (ipsilateral hand).
Related QuestionsWhat is a "locked-in" syndrome?
Frequently Asked Questions about Mild and Severe Brain Injur...For a long time we thought that individuals who were in a state of diminished consciousness were unable to respond. Through years of working with people with severe brain injuries and diminished responding capacities we have learned that the person may be receiving information but be unable to produce an effective response. Some people may communicate with an eye blink, a facial gesture or even by moving a toe.
Related QuestionsWhat is Metabolic Syndrome?
Rite Aid : Faq'sMetabolic Syndrome is a group of disorders and symptoms that when present increases ones risk of coronary artery disease and stroke. These disorders include: Abdominal obesity (where waist circumference is greater than 40 inches in men and greater than 35 inches in women) It starts with insulin resistance, which is a reduced sensitivity of the body's tissues—primarily the liver and muscles—to the action of insulin. The following FAQ explains this:
Related QuestionsWhat is Post Embolization Syndrome?
Fibroid Frequently Asked QuestionsAbout 40% of women experience PES. It is a result of tissue necrosis from the infarcted myomata. PES is characterized by pain, fever, high white blood cell count, nausea and vomiting. This should be followed closely to distinguish it from a complicating infection.
Related QuestionsWhat is Leriche's syndrome?
Peripheral Arterial Disease of the Legs, SVCMC; New York NYMany things can increase your risk for developing atherosclerosis and peripheral arterial disease (PAD). These include: Call your doctor immediately if you have a sudden onset of leg pain, numbness, or pale, blue-black skin. Leg pain that begins after walking a certain distance and goes away when you rest (intermittent claudication). Taking a wait-and-see approach, called watchful waiting, is not appropriate for peripheral arterial disease.
Related QuestionsHow common is overactive bladder syndrome?
Overactive Bladder Information - Signs and SymptomsIn two large studies it was found that about 1 in 6 adults reported some symptoms of an overactive bladder. Symptoms vary in their severity. About 1 in 3 people with an overactive bladder have episodes of urge incontinence.
Related QuestionsWhat is irritable bowel syndrome?
Health InformationIrritable bowel syndrome is one of the manifestations of functional abdominal pain. Functional means that there is no organic disease. Functional abdominal pain describes a constellation of symptoms as a result of intestinal motility disorders. Symptoms may include:
Related QuestionsWhat causes irritable bowel syndrome?
Health InformationThe digestion and propulsion of nutrients and fluids through the gastrointestinal system (GI) is a very complicated and very well organized process. The GI tract has its own intrinsic muscles and nerves that connect, like an electrical circuit, to the spinal cord and brain. Neuromuscular events occurring in the GI tract is relayed to the brain through neural connections, and the response of the brain is also relayed back to the gastrointestinal tract.
Related QuestionsWho is affected by irritable bowel syndrome?
Health InformationThirty-three percent of adults who have irritable bowel syndrome can trace their symptoms back to childhood. There is no known gene that causes irritable bowel syndrome, but the disorder does seem to occur more often in families where either a child or a parent has the disorder.
Related QuestionsWhy is irritable bowel syndrome a concern?
Health InformationChildren with irritable bowel syndrome often do not feel well. Those who have diarrhea may have little warning of their need to go to the bathroom, and, therefore, may be embarrassed and avoid going to school or socializing with their schoolmates. Children can become depressed or anxious because of the disorder. Most children with irritable bowel syndrome continue to grow and develop normally.
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