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Frequently Asked Questions

How is PWS diagnosed?

QUESTIONS AND ANSWERS ON PRADER-WILLI SYNDROME
Suspicion of the diagnosis is first assessed clinically, then confirmed by specialized genetic testing on a blood sample. Formal diagnostic criteria for the clinical recognition of PWS have been published (Holm et al, 1993), as have laboratory testing guidelines for PWS (ASHG, 1996).
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Prader Willi Syndrome - PWS Network
There are clinical criteria for a diagnosis of PWS, but chromosome analysis provides the most reliable and useful diagnosis. back to top
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Is PWS inherited?

QUESTIONS AND ANSWERS ON PRADER-WILLI SYNDROME
Most cases of PWS are attributed to a spontaneous genetic error that occurs at or near the time of conception for unknown reasons. In a very small percentage of cases (2 percent or less), a genetic mutation that does not affect the parent is passed on to the child, and in these families more than one child may be affected. A PWS-like disorder can also be acquired after birth if the hypothalamic portion of the brain is damaged through injury or surgery.
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How common is PWS?

QUESTIONS AND ANSWERS ON PRADER-WILLI SYNDROME
It is estimated that one in 12,000 to 15,000 people has PWS. Although considered a "rare" disorder, Prader-Willi syndrome is one of the most common conditions seen in genetics clinics and is the most common genetic cause of obesity that has been identified. PWS is found in people of both sexes and all races.
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How can I get more information about PWS?

QUESTIONS AND ANSWERS ON PRADER-WILLI SYNDROME
A strong national organization of families and professionals, PWSA (USA) offers a toll-free helpline, a bimonthly member newsletter and numerous publications about PWS, a World Wide Web page (www.pwsausa.org), an annual family conference and scientific meeting, and chapters throughout the country to provide local family support and advocacy.
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How it is diagnosed?

Laparoscopy Hospital - Frequently asked questions about lapa...
Several ways have been suggested to diminish the diagnostic error that occurs if diagnosis is based solely on the clinical picture of suspected appendicitis. In fact appendicitis is a disease, which can mimic most of the causes of abdominal pain as well as some of the chest diseases. Despite new x-ray techniques, CT scans and ultrasounds, the diagnosis of appendicitis can be quite challenging.
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Vulvodynia: Vulvar Pain Clinics: FAQ's Vestibulitis, Vestibu...
Exquisite sensitivity of the tiny gland openings at the entrance of the vagina, to light touch with a cotton-tipped applicator, is the typical diagnostic feature of Vulvodynia. This is called the “touch test.” About two thirds of patients with Vulvodynia have visible, red tiny spots at these points. For the remainder of patients, a doctor may detect inflamed surface blood vessels with a colposcope, which is a magnifying instrument.
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Arthritis NSW | Education | Frequently Asked Questionsa abou...
Each year a large number of people visit their General Practitioner (GP) with symptoms such as back pain, neck pain, muscle pain or swollen and painful joints. Often, these symptoms are not severe and may last just a few days, in which case the GP will provide advice or treatment and allow the problem to resolve. But, if the pain persists or is severe, your GP may decide to refer you to a specialist in musculoskeletal diseases.
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Vanishing Twin Syndrome - Answers to Frequently Asked Questi...
Here's a typical scenario: A mother undergoes a routine ultrasound early in her pregnancy, for example at six or seven weeks gestation. Two fetuses are detected. The mother is told she is having twins. When the mother returns to the doctor six weeks later, only one heartbeat can be heard with a Doppler scan. Another ultrasound is performed. Only one fetus is identified.
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EndoFAQ
The only way a positive diagnosis of Endo can be made currently is via surgery, either a laparoscopy or the more invasive laparotomy, where biopsies are taken from suspected sites. It can also be visualized during surgery if the surgeon knows what to look for. Ultrasounds, MRIs, CT Scans and other diagnostic tests are not conclusive. The ERC does not support "medical diagnoses," such as administering GnRH therapy prior to a surgical diagnosis.
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PROLEUKIN® (aldesleukin): FAQs About Kidney Cancer
Kidney cancer is usually diagnosed using magnetic resonance imaging (MRI) or ultrasound imaging, or by tissue biopsy. (Please see Kidney Cancer Diagnosis for more information.)
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What is Prader-Willi syndrome (PWS)?

QUESTIONS AND ANSWERS ON PRADER-WILLI SYNDROME
PWS is a complex genetic disorder that typically causes low muscle tone, short stature, incomplete sexual development, cognitive disabilities, problem behaviors, and a chronic feeling of hunger that can lead to excessive eating and life-threatening obesity.
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What causes the appetite and obesity problems in PWS?

QUESTIONS AND ANSWERS ON PRADER-WILLI SYNDROME
People with PWS have a flaw in the hypothalamus part of their brain, which normally registers feelings of hunger and satiety. While the problem is not yet fully understood, it is apparent that people with this flaw never feel full; they have a continuous urge to eat that they cannot learn to control. To compound this problem, people with PWS need less food than their peers without the syndrome because their bodies have less muscle and tend to burn fewer calories. No.
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Do diet medications work for the appetite problem in PWS?

QUESTIONS AND ANSWERS ON PRADER-WILLI SYNDROME
Unfortunately, no appetite suppressant has worked consistently for people with PWS. Most require an extremely low-calorie diet all their lives and must have their environment designed so that they have very limited access to food. For example, many families have to lock the kitchen or the cabinets and refrigerator.
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What kinds of behavior problems do people with PWS have?

QUESTIONS AND ANSWERS ON PRADER-WILLI SYNDROME
In addition to their involuntary focus on food, people with PWS tend to have obsessive/compulsive behaviors that are not related to food, such as repetitive thoughts and verbalizations, collecting and hoarding of possessions, picking at skin irritations, and a strong need for routine and predictability. Frustration or changes in plans can easily set off a loss of emotional control in someone with PWS, ranging from tears to temper tantrums to physical aggression.
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What does the future hold for people with PWS?

QUESTIONS AND ANSWERS ON PRADER-WILLI SYNDROME
With help, people with PWS can expect to accomplish many of the things their "normal" peers do—complete school, achieve in their outside areas of interest, be successfully employed, even move away from their family home. They do, however, need a significant amount of support from their families and from school, work, and residential service providers to both achieve these goals and avoid obesity and the serious health consequences that accompany it.
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What other services can I get from PWS?

ADPUSH - FAQ
We are working to bring our affiliates guest books, message boards, and free-for-all link services in the very near future. Stay tuned!
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How are allergies diagnosed?

Allergy Frequently Asked Questions (FAQ)
allergist or immunologist can diagnose your allergies using allergy skin tests, which show if your immune system reacts to specific allergens. You can also test your reactivity to common allergens using a home allergy test.
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How is CFS diagnosed?

GWVRP: Document Detail
When evaluating patients with chronic fatigue of unknown origin, physicians can use the following definition of CFS as a guide. This detailed definition was developed for research use under the leadership of the Centers for Disease Control. It was published in the "Annals of Internal Medicine" in March 1988. Because the disease is still poorly understood, however, the outlined criteria should be considered provisional.
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How is SAD diagnosed?

Seasonal Affective Disorder (SAD), SVCMC; New York NY
A doctor will base his or her diagnosis of SAD on whether you have been depressed in the winter and recovered in the spring or summer for at least 2 years in a row. These dramatic mood swings in response to changes in seasons are what differentiate SAD from nonseasonal depression.
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How is Hyperhidrosis diagnosed?

Revita Medispa :: Frequently asked questions
A:The area of increased sweating is determined by a simple method. A weak solution of iodine is applied to the skin under the arms and then a dusting of powdered starch is applied over the iodine. This mixture will turn blue in the areas of excessive sweating allowing the physician to know where to inject the BOTOX®. These blue marks will be cleaned off after your treatment.
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How is CWD diagnosed?

Chronic Wasting Disease FAQs - Department of Agriculture, Tr...
The only sure way to diagnose CWD is to examine the animal’s brain for the characteristic lesions that make the brain look like a sponge. There is no approved test for live animals, although one is in development.
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What if I have already been diagnosed or treated?

The Sleep Advisor Frequently Asked Questions
Because The Sleep Advisor uses an integrative approach that blends the best of conventional sleep health with proven complementary and alternative medicine, most users receive a much more comprehensive set of recommendations than they might have previously received. People already diagnosed with insomnia and sleep apnea, for example, often receive important and useful recommendations to enhance and improve the effectiveness of their current treatment.
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How is anorexia diagnosed?

Quality Health | Anorexia Nervosa
If your doctor thinks that you may have an eating disorder, he or she will compare your weight with the expected weight for someone of your height and age. He or she will also check your heart, lungs, blood pressure, skin, and hair to look for problems caused by not eating enough. You may also have blood tests or X-rays. Your doctor may ask questions about how you feel. It is common for a treatable mental health problem such as depression or anxiety to play a part in an eating disorder.
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How is ADHD diagnosed?

Duke ADHD Program – Frequently Asked Questions
The diagnosis of ADHD can be made reliably using well–tested diagnostic interview methods. Diagnosis is based on history and observable behaviors in the child’s usual settings. Ideally, a health care practitioner making a diagnosis should include input from parents and teachers.
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How is BPH diagnosed?

Benign Prostatic Hyperplasia (BPH)
Your doctor can diagnose BPH by asking questions about your symptoms and past health and by doing a physical exam. Tests may include a digital rectal exam, which lets your doctor feel the size of your prostate, and a urine test (urinalysis). In some cases, a prostate-specific antigen (PSA) test is done to help rule out prostate cancer. (Prostate cancer and BPH are not related, but they can cause some of the same symptoms.
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How is PKD Diagnosed?

The Feline PKD FAQ -- Answers to Frequently Asked Questions ...
Currently, the best method to diagnose PKD in living cats is by ultrasounding the kidneys. Other radiological modalities have been used, but have proven to be generally less accurate and more costly. However, even the most skilled sonographer using the best equipment cannot be 100 percent accurate in diagnosing PKD via ultrasound, since the resolution afforded by ultrasound is not sufficient to detect very small cysts.
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How Are Clients Diagnosed?

Connections: Health.Wellness.Advocacy
The diagnosis process begins with an intial call by the client to the Agency. Once and appointment is set up the client will come in for a comprehensive assessment. This assessment consists of a medical/physical screen, a psychosocial history, presenting problems, treatment history and financial assessment.
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