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Prader-willi Syndrome:     more books (67)

A pragmatic profile of individuals diagnosed with Prader-Willi syndrome by Lisa J Vikla, 1992 The Prader-Labhart-Willi syndrome: Review of the literature andreport of nine cases, (Acta pædiatrica Scandinavica. Supplement) by Henry G Dunn, 1968 Anticipatory guidance for parents of Prader-Willi children.(Continuing Education Series): An article from: Pediatric Nursing by Mary Ellen Nolan, 2003-11-01 Pediatric Endocrinology: A Practical Clinical Guide (Contemporary Endocrinology) Chromosomal abnormalities: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Michelle, MS, CGC Bosworth, 2005 Obesity Before Birth: Maternal and prenatal influences on the offspring (Endocrine Updates) Sometimes I'm mad, sometimes I'm glad: ... on being a Prader-Willi family by Janalee, 1982 Prader Willi: A guide for professionals in education by Stacey R Pumper, 1998 A common-sense approach to dietary management of the Prader-Willi person: A paper Autism:Beyond the Basics by William Shaw Ph.D., Kurt Woeller D.O., et all 2010-05-04 Princess Polly and the Magic Doll by Valerie Hall, 2008-04-01

lists with details

81. The DRM WebWatcher: Prader-Willi Syndrome (PWS)
    praderwilli syndrome (PWS) is a group of symptoms caused by a genetic defect in Chromosome 15. PWS occurs in about one of every 15,000 births.  
    http://www.disabilityresources.org/PWS.html
    
    Extractions: Home Subjects States Librarians ... Contact Us The DRM WebWatcher Prader-Willi Syndrome (PWS) Updated 3/2004 A B C D ... About/Hint/Link Prader-Willi Syndrome (PWS) is a group of symptoms caused by a genetic defect in Chromosome 15. PWS occurs in about one of every 15,000 births. Symptoms of Prader-Willi Syndrome can include impaired body control, mental retardation, hypotonia during infancy, short stature, insatiable appetite beginning after infancy, scratching and skin picking, and behavior difficulties. Check these sites for more information. Prader-Willi Syndrome This technical page from GeneClinics includes in-depth clinical and genetic information. Prader-Willi Syndrome Association The Association's web site offers basic information about the syndrome, research news, personal stories and family support (including chat and message board), and links, as well as information about the organization, its chapters, and its publications. Prader-Willi Syndrome Association (UK) This British organization offers "An A to Z of PWS," genetic information, portraits of people with PWS, and information for people with PWS and for sibling. Related Subjects Growth Disorders Mental Retardation Rare Disorders Resources in your state (c) 1997-2001 Disability Resources, inc.

82. Prader-willi Syndrome - General Health Information - Prader_willi Syndrome Is A
    praderwilli syndrome - General Health Information. prader-willi syndrome - General Health Information. Home Weight Loss prader-willi syndrome.  
    http://www.allhealthlinks.com/dir/395/1.php
    
    Extractions: Click below for more info: google_ad_client = 'pub-2815073187333366'; google_ad_width = 300; google_ad_height = 250; google_ad_format = '300X250_as'; google_ad_channel = '3846168253'; google_color_border = "f7f7f7"; google_color_bg = "f7f7f7"; google_color_link = "blue"; google_color_url = "blue"; google_color_text = "000001"; Related Keywords Cross-referenced categories in "Prader-willi syndrome - General Health Information": Articles Chat Coupons Deals ... United States Results 1 - 10 of 23 found in "Prader-willi syndrome - General Health Information": Website of the Prader-Willi Syndrome Association of South Africa Website of the Prader-Willi Syndrome Association of South Africa http://www.praderwilli.org.za

83. Prader-willi Syndrome - Tools - Prader_willi Syndrome Is A Disorder Which Is Som
    praderwilli syndrome - Tools. prader-willi syndrome - Tools. Home Weight Loss prader-willi syndrome. General Health Information Tools.  
    http://www.allhealthlinks.com/dir/395/307.php
    
    Extractions: Click below for more info: google_ad_client = 'pub-2815073187333366'; google_ad_width = 300; google_ad_height = 250; google_ad_format = '300X250_as'; google_ad_channel = '3846168253'; google_color_border = "f7f7f7"; google_color_bg = "f7f7f7"; google_color_link = "blue"; google_color_url = "blue"; google_color_text = "000001";

84. PRADER-WILLI SYNDROME
    Features Listed For praderwilli syndrome. McKusick 176270. Diabetes mellitus/hyperglycaemia; Generalized obesity; Hypertension; Microcephaly;  
    http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?1384

85. Health, Conditions And Diseases, Genetic Disorders: Prader-Willi Syndrome
    Gretton Homes Information about the organization that offers residential care for people with prader-willi syndrome. Ontario Prader  
    http://www.combose.com/Health/Conditions_and_Diseases/Genetic_Disorders/Prader-W
    
    Extractions: Related links of interest: Health:Mental Health:Disorders:Neurodevelopmental:Autism Spectrum Health:Mental Health:Disorders:Child and Adolescent:Mental Retardation:Causes Health:Conditions and Diseases:Neurological Disorders:Chromosomal Health:Conditions and Diseases:Nutrition and Metabolism Disorders:Obesity ... Gretton Homes - Information about the organization that offers residential care for people with Prader-Willi Syndrome. Ontario Prader-Willi Syndrome Association - OPWSA provides support and information to all those interested in finding out about this syndrome. A special emphasis on Canadian content. Prader-Willi Alliance of New York - Represents the interests of individuals in New York State with Prader-Willi syndrome, their families, and the professionals who provide services to the Prader-Willi population. Prader-Willi Syndrome - Suite101 - A forum to provide a support base for PWS without having to join one of the national or international associations, and to make people more aware of PWS. Prader-Willi Syndrome Association (USA) - Characteristics include hypotonia, insatiable appetite, obesity if food intake is uncontrolled, hypogonadism and incomplete sexual development, developmental delays, variable degrees of mental retardation or functional retardation, short stature (adult), small hands and feet, mild dysmorphology, and behavior problems which can be severe.

86. Support - Prader-Willi Syndrome Association - Everybody.co.nz
    praderwilli syndrome Association of NZ. WHAT IS prader-willi syndrome? CONTACT DETAILS. prader-willi syndrome Association (NZ) Inc. Annual membership is NZ$20.  
    http://www.everybody.co.nz/support/prader-w.html

87. Prader-Willi Syndrome Definition Meaning Information Explanation
    praderwilli syndrome. - definition Babies with prader-willi syndrome are born with low muscle tone and a weak sucking reflex. Once  
    http://www.free-definition.com/Prader-Willi-syndrome.html
    
    Extractions: Google News about your search term Prader-Willi syndrome is a genetic disorder in which seven genes (or some subset thereof) on chromosome 15 are missing or unexpressed ( chromosome 15q, partial deletion ). It was discovered in by Andrea Prader, Heinrich Willi, Alexis Labhart, and Guido Fanconi of Switzerland Babies with Prader-Willi syndrome are born with low muscle tone and a weak sucking reflex. Once the muscles strengthen, however, their insatiable appetite takes over. They eat and eat, never feeling full. As they have a lower metabolism than normal people, they often end up obese if the kitchen isn't locked. This is caused by a misdevelopment of the hypothalamus The genes of Prader-Willi syndrome are expressed only on the paternal chromosome. The eighth gene in the segment, whose deletion causes Angelman syndrome , is expressed only on the maternal chromosome. It is thus possible for a woman with Prader-Willi syndrome to pass the mutation to her son, who has Angelman syndrome. This is the first known instance of imprinting in humans.

88. Pathology Molecular Genetics Prader-Willi Syndrome
    INDICATIONS FOR TESTING praderwilli syndrome is characterized by severe hypotonia and feeding difficulties in early infancy, followed by uncontrolled  
    http://www.allkids.org/Specialties/Pathology/Pages/Molecular_Genetics_Prader_Wil
    
    Extractions: Prader-Willi syndrome is characterized by severe hypotonia and feeding difficulties in early infancy, followed by uncontrolled appetite and severe obesity in childhood. All patients have mild to moderate mental retardation and often behavioral problems. Patients have hypogonadism and infertility. This disorder is caused by paternally derived deletions of chromosome 15q11-q12 (~70% of cases), by uniparental maternal disomy of chromosome 15 (~25%), by chromosomal translocations (~1%) or by unknown etiology (~5%).

89. Prader Willi Syndrome Info Brief
    Information Brief on Developmental Disabilities. 1998. praderwilli syndrome. prader-willi syndrome is a rare birth defect. Causes of prader-willi syndrome.  
    http://www.moddrc.com/Information-Disabilities/FastFacts/prader.htm
    
    Extractions: Developmental Disabilities Prader-Willi Syndrome Prader-Willi Syndrome is a rare birth defect. About 1 in 14,000 babies are born with Prader-Willi Syndrome. Characteristics of Prader-Willi Syndrome include decreased muscle tone, developmental delays, insatiable appetite, incomplete sexual development, short adult stature, small hands and feet, and severe behavior problems. Infants with Prader-Willi Syndrome are usually of normal size. They have weak muscle tone and poor reflexes. Because they are unable to suck well, they often have to be fed through a tube, or fed with special nipples. They tend to be lethargic, and have a weak cry. As babies age, developmental delays are common. Sitting may occur when babies are about a year old. Walking is usually accomplished at the age of two. Language development is often delayed, and articulation poor. Compulsive eating usually begins between the ages of two to four, occasionally beginning as late as six. People with Prader-Willi have an insatiable desire for food. Sneaking food and stealing food are common. If allowed to eat as much as they want, most people with Prader-Willi Syndrome become considerably overweight. A dysfunction in the part of the brain called the hypothalamus keeps them from knowing when they have had enough to eat, and keeps them craving food.

90. Prader-Willi Syndrome
    Phenylketonuria (PKU). praderwilli syndrome. Urea Cycle Defects. prader-willi syndrome. See this excellent site for information http//www.pwsausa.org/.  
    http://www.vanhosp.bc.ca/html/wellness_amdc_findout_prader.html

91. Genetic Disorders, Prader-Willi Syndrome
    More praderwilli syndrome Categories » Submit Your Site to the prader-willi syndrome category. Submit Your Site to the prader-willi syndrome category.  
    http://www.iseekhealth.com/prader-willi_syndrome-1611.php
    
    Extractions: Gretton Homes - Information about the organization that offers residential care for people with Prader-Willi Syndrome. Ontario Prader-Willi Syndrome Association - OPWSA provides support and information to all those interested in finding out about this syndrome. A special emphasis on Canadian content. Prader-Willi Alliance of New York - Represents the interests of individuals in New York State with Prader-Willi syndrome, their families, and the professionals who provide services to the Prader-Willi population. Prader-Willi Syndrome - Suite101 - A forum to provide a support base for PWS without having to join one of the national or international associations, and to make people more aware of PWS. Prader-Willi Syndrome Association (USA) - Characteristics include hypotonia, insatiable appetite, obesity if food intake is uncontrolled, hypogonadism and incomplete sexual development, developmental delays, variable degrees of mental retardation or functional retardation, short stature (adult) Prader-Willi Syndrome Association of Victoria (Australia) - Includes details about the organization, a diagnosis/infant guide, a general guide, members stories and links.

92. The Children's Institute
    praderwilli syndrome. Our inpatient hospital program for both children and adults with prader-willi syndrome is the only one of its kind in the country.  
    http://www.amazingkids.org/dg_11.asp
    
    Extractions: Providing integrated medical and behavioral crisis intervention to persons with Prader-Willi Syndrome Our inpatient hospital program for both children and adults with Prader-Willi Syndrome is the only one of its kind in the country. Since 1981, more than 800 children and adults with Prader-Willi Syndrome from the United States and Canada have benefited from this program. The Institute Provides: These types of crises usually overlap and often occur simultaneously in persons with PWS making treatment in a less specialized setting difficult or impossible. (General pediatric or adult psychiatric units, medical units, medical ICUs, PICUs, ICFMRs, nursing homes etc. are not prepared to address the complex needs of patients with PWS.)

93. Prader-Willi Syndrome - The Knowledge Database Of The Swedish National Board Of
    praderwilli syndrome. To the Swedish version prader-willi syndrome and other Chromosome 15q Deletion Disorders. NATO ASI Series Springer Verlag, 1992.  
    http://www.sos.se/smkh/2002-110-4/2002-110-4.htm
    
    Extractions: With effect from 2001, the National Board of Health and Welfare classifies its publications into various types of document. This an Overview of Knowledge . That means that the report is based on science and/or proven experience. Overviews of knowledge among other things are to provide support for knowledge-based care and treatment, method development and other improvement work, encourage and facilitate quality follow-up and/or encourage efficient utilisation of resources. The National Board of Health and Welfare is responsible for the contents and conclusions. The disease/injury/diagnosis Article number: 2002-110-4 English index Search The aphabetical list This is an excerpt from the knowledge database of the Swedish National Board of Health and Welfare on rare diseases. The concept of "rare diseases" is defined as: "Disorders or injuries resulting in extensive handicaps and affecting no more than 100 individuals in one million inhabitants". The ambition underlying the database is to provide up-to-date information on rare diseases and about the support and services these groups of people require. Prader-Willi Syndrome (PWS) was described for the first time in 1956. The syndrome was named by the group of Swiss paediatricians who first identified a number of patients with the combination of excessive body weight, mental retardation, short stature, abnormally low production of sexual hormones (hypogonadism) and low muscle tone at birth.

94. BabyCenter | Community: BBS - Chromosome Disorders | Prader-Willi Syndrome
    Author kiddie420, May 5, 2004, 221 PM (PDT), Hello, my son was born 04/16/04 and has praderwilli syndrome. I had no idea anything was wrong until he was born.  
    http://bbs.babycenter.com/board/baby/babyills/1378212/thread/1013956
    
    Extractions: Preconception Pregnancy Baby ... Chromosome disorders "Prader-Willi Syndrome" Posts: Last Post: May 19, 2004, 8:14 AM (PDT) JOIN IN: See all Boards Create a new thread Add a message WATCHES: My watches Start watching this thread HOW TO: Getting started Community Guidelines Back to Chromosome disorders Messages First Last Author: kiddie420 May 5, 2004 , 2:21 PM (PDT) Hello, my son was born 04/16/04 and has Prader-Willi Syndrome. I had no idea anything was wrong until he was born. He will have a hard time with controlling eating and will also have learning and behavioral problems but we are ready to handle whatever may come our way and give him the best life possible. It's easy now because he's a baby and lots of the problems show up in a year or two. I hope some time there will be someone else on this board with a child with PWS, not likely I guess because it's pretty rare. (about one in 12,000 - 15,000 people have it) Just wanted to join in the new board and give everyone an idea of what PWS is! I'm very excited about this board! Add a post Quote this post Author: Lemony May 5, 2004

95. CPS: CPSP Prader-Willi Syndrome
    praderwilli syndrome Principal investigator. Nita Goldband, Executive Director, Ontario prader-willi syndrome Association. Study publications/presentations.  
    http://www.cps.ca/english/CPSP/Studies/prader.htm
    
    Extractions: Prader-Willi syndrome Principal investigator Glenn B. Berall, BSc, MD, FRCPC, Chief of Paediatrics, North York General Hospital, 4001 Leslie St., Toronto, ON M2K 1E1; tel.: 416-756-6222; fax: 416-756-6853; e-mail: gberall@nygh.on.ca Co-investigators Maria Virginia Desantadina, MD, Paediatrician, Research Fellow, Department of Nutritional Sciences, University of Toronto, The Hospital for Sick Children. Consultant Nita Goldband, Executive Director, Ontario Prader-Willi Syndrome Association Study publications/presentations CPSP highlights Presentations Genetic studies: A significant component of the Canadian Paediatric Surveillance Program. Challenging behavioural problems in children with genetic and rare conditions: Role of the Canadian Paediatric Surveillance Program. Public health implications of the Candadian Paediatric Surveillance Program. International Network of Paediatric Surveillance Units: A child's global village. Workshop on Puberty in CHARGE and General Endocrine Issues in CHARGE. Blake K. Presented at the 6th International CHARGE Syndrome Conference, Cleveland, Ohio, July 25 to 27, 2003. Surveillance helping patients with orphan genetic disorders. MV Desantadina, KD Blake, MJM Nowaczyk. Presented at the he 80th Annual Meeting of the Canadian Paediatric Society, Calgary, June 21, 2003.

96. Disease - Prader-Willi Syndrome - Hartford, Connecticut , Saint Francis Care
    Disease prader-willi syndrome. Growth hormone has also been shown to inprove physical strength and agility in patients with prader-willi syndrome.  
    http://www.saintfranciscare.com/13350.cfm
    
    Extractions: Back Back to main Health Information page Hypotonia Definition: Prader-Willi syndrome is a congenital (present from birth) disease characterized by obesity decreased muscle tone , decreased mental capacity, and hypogonadism Causes And Risk: Prader-Willi is caused by the deletion of a gene on chromosome 15. For unkown reasons, only the copy of this gene on chromosome 15 that is received from the father is active. The maternal copy of this gene is turned off in all people. When there is a deletion of this gene on the copy received from the father, the disease occurs. This is because the patient is left with only the maternal copy which is inactive in all people. Signs of Prader-Willi may be seen at birth. New infants with the condition are often small and very floppy (hypotonic). Male infants may have undescended testicles . The growing child exhibits slow mental and delayed motor development, increasing obesity , and characteristically small hands and feet.

97. Tokyo Medical University Genetics Prader-Willi Syndrome References
    ·? ( praderwilli syndrome ). 6. Butler, MG prader-willi syndrome current understanding of cause and diagnosis. Am. J. Med.  
    http://www.tokyo-med.ac.jp/genet/pws/pwsjref.htm
    
    Extractions: 3. Buiting, K.; Dittrich, B.; Gross, S.; Greger, V.; Lalande, M.;Robinson, W.; Mutirangura, A.; Ledbetter, D.; Horsthemke, B. : Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene. Hum. Molec. Genet. 4. Burke, C. M.; Kousseff, B. G.; Gleeson, M.; O'Connell, B. M.; Devlin,J. G. : Familial Prader-Willi syndrome. Arch.Intern. Med.

98. Prader-Willi Syndrome (PWS) - FISH Analysis
    praderwilli syndrome (PWS) FISH ANALYSIS See also prader-willi syndrome - DNA Analysis.  
    http://www.bcmgeneticlabs.org/tests/cyto/praderwilli_fish.html
    
    Extractions: See also: Prader-Willi Syndrome - DNA Analysis Open Page in New Window Print This Page Return to Search The Kleberg Cytogenetics Laboratory offers a fluorescence in situ hybridization (FISH)-based assay for identifying the deletion on chromosome 15q11-q13 associated with Prader-Willi syndrome. Clinical Features: Patients with clinical features suggestive of Prader-Willi syndrome may be tested for deletions of 15q11-q13 by FISH simultaneously with high-resolution chromosomal analysis (if not previously performed). FISH may also be indicated when methylation studies have shown deficiency of the paternal unmethylated allele. Prenatal diagnosis may be performed if an affected family member has been studied in our laboratory and shown to have a deletion detectable by FISH. Please call regarding all prenatal samples. Testing Methodology:

99. Uniparental Disomy: Prader-Willi Syndrome, Angelman Syndrome
    Resources Uniparental Disomy praderwilli syndrome, Angelman Syndrome. What is uniparental disomy? What is prader-willi syndrome (PWS)? Prader  
    http://www.stlouischildrens.org/articles/content.asp?pageid=P02159

100. ORPHANET - Maladies Rares - Médicaments Orphelins
     Translate this page Version pour Impression, MALADIE prader-willi, syndrome de, Synonyme(s) Willi-Prader, syndrome de, CIM Q87.1, Le syndrome de Prader  
     http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=739

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