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williams syndrome - rare genetic disease with increased calcium levels and heart disease Definition for Williams Syndrome Williams syndrome (also Williams-Beuren syndrome, sometimes called Pixieism) is a rare genetic disorder, occurring in fewer than 1 in 7,500 live births.It is characterized by a distinctive, "elvish" facial appearance, along with a low nasal bridge; an unusually cheerful demeanor and ease with strangers, coupled with unpredictably occurring negative outbursts; mental retardation coupled with unusual (for persons who are diagnosed as mentally retarded) language skills; a love for music; and cardiovascular problems, such as supravalvular aortic stenosis and transient hypercalcaemia. some common symptoms abnormal gait delayed development high blood pressure poor social skills some related diagnoses 1 - 7 of 21 diagnoses drugs and toxins neurofibromatosis type 1 Hartnup disease urea cycle disorders human immunodeficiency virus infections malnutrition hydrocephalus   more do i have 'Williams Syndrome'? In addition the following diagnostic tests might be need to help verify the diagnosis: diagnostic test search results for 'williams syndrome' 1 - 5 of 30 diagnostic tests Amniocentesis Williams Syndrome and Amniocentesis Chorionic Villus Sampling (CVS) Williams Syndrome and Chorionic Villus Sampling (CVS) Chromosomal analysis Williams Syndrome and Chromosomal analysis Fluorescent in situ hybridization (FISH) Williams Syndrome and Fluorescent in situ hybridization (FISH) BUN Williams Syndrome and BUN Complete metabolic panel Williams Syndrome and Complete metabolic panel Dental x-rays Williams Syndrome and Dental x-rays ECHOcardiogram Williams Syndrome and ECHOcardiogram EKG Electrocardiogram Williams Syndrome and EKG Hearing test standard technique of representing hearing loss Williams Syndrome and Hearing test KUB Williams Syndrome and KUB Psychometric testing Williams Syndrome and Psychometric testing Serum Creatinine Williams Syndrome and Serum Creatinine Serum calcium Williams Syndrome and Serum calcium Ultrasonography kidneys ureter bladder Williams Syndrome and Ultrasonography kidneys ureter bladder Urinalysis Examination of urine to detect disease Williams Syndrome and Urinalysis bone age Williams Syndrome and bone age urine calcium creatinine ratio Williams Syndrome and urine calcium creatinine ratio vision tests Williams Syndrome and vision tests Serum Creatine Kinase (CK) Williams Syndrome and Serum Creatine Kinase (CK) Cardiac Catheterization coronary angiogram Williams Syndrome and Cardiac Catheterization Serum TSH Williams Syndrome and Serum TSH Serum phosphorus Williams Syndrome and Serum phosphorus Comprehensive eye exam Williams Syndrome and Comprehensive eye exam Developmental testing Williams Syndrome and Developmental testing Neuropsychiatric evaluation Williams Syndrome and Neuropsychiatric evaluation Psychologic Evaluation and support Williams Syndrome and Psychologic Evaluation and support Urinary electrolytes Williams Syndrome and Urinary electrolytes serum electrolytes Williams Syndrome and serum electrolytes speech reception threshold (SRT) Williams Syndrome and speech reception threshold (SRT) for more please login, login is free (click to login) therapeutic procedures for 'Williams Syndrome'? Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for Williams Syndrome: therapeutic procedure search results for 'williams syndrome' 1 - 5 of 8 therapeutic procedures rankings are computer generated. please consult your health care provider. Cardiac surgery Williams Syndrome and Cardiac surgery restriction of vitamin D in diet Williams Syndrome and restriction of vitamin D in diet Physical and Occupational Therapy Arthritis Physical and Occupational Therapy Williams Syndrome and Physical and Occupational Therapy Restriction dietary calcium Williams Syndrome and Restriction dietary calcium Special Education Williams Syndrome and Special Education Speech Therapy Williams Syndrome and Speech Therapy dental care Williams Syndrome and dental care diet modification Williams Syndrome and diet modification for more please login, login is free (click to login) medications search results for 'williams syndrome' 1 - 1 of 1 medications rankings are computer generated. please consult your health care provider.   bisphosphonates Williams Syndrome and bisphosphonates web search results for williams syndrome Web (All)  |  Treatment  |  Drugs  |  Tests  |  Research  |  Diet Results 1 - 50 - Williams Syndrome Williams syndrome Williams syndrome is a rare genetic disorder that can lead to problems ... a person with Williams syndrome has a 50% chance ... Williams Syndrome ... http://adam.about.com/encyclopedia/infectiousdiseases/Williams-syndrome.htm   adam.about.com - summary Williams syndrome - Wikipedia, the free encyclopedia Individuals with Williams syndrome are highly verbal and sociable, but lack ... Viewing it differently: Social scene perception in Williams syndrome and Autism" ... http://en.wikipedia.org/wiki/William's_syndrome   en.wikipedia.org - summary Williams syndrome - Genetics Home Reference Williams syndrome is a developmental disorder that affects many parts of the body. ... People with Williams syndrome typically have difficulty with visual-spatial ... http://ghr.nlm.nih.gov/condition=williamssyndrome   ghr.nlm.nih.gov - summary Williams Syndrome - Yahoo! Health Important It is possible that the main title of the report Williams Syndrome is not the name you expected. Please check the synonyms listing to find the alternate ... http://health.yahoo.com/ency/healthwise/nord298   health.yahoo.com - summary Williams Syndrome Williams Syndrome (WS) is a rare genetic disorder characterized by mild to ... There is no cure for Williams syndrome, nor is there a standard course of treatment. ... http://www.clevelandclinic.org/health/health-info/docs/1300/1361.asp?index=   www.clevelandclinic.org - summary Williams Syndrome -- GeneReviews -- NCBI Bookshelf Williams syndrome (WS) is characterized by cardiovascular disease (elastin ... Williams syndrome is transmitted in an autosomal dominant manner. ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams   www.ncbi.nlm.nih.gov - summary MedlinePlus Medical Encyclopedia: Williams syndrome Williams syndrome is a rare condition caused by missing genes. ... a person with Williams syndrome has a 50 ... Williams Syndrome Foundation -- www.wsf.org ... http://www.nlm.nih.gov/medlineplus/ency/article/001116.htm   www.nlm.nih.gov - summary Williams syndrome - Wikipedia, the free encyclopedia People with Williams syndrome often have hyperacusis and phonophobia which ... Williams syndrome is caused by the deletion of genetic material from the region ... http://en.wikipedia.org/wiki/Williams_syndrome   en.wikipedia.org - summary Williams syndrome Although individuals with Williams syndrome may show competence in areas such as ... In Williams syndrome individuals, both the gene for elastin and an enzyme called ... http://www.ncbi.nlm.nih.gov/disease/Williams.html   www.ncbi.nlm.nih.gov - summary Williams syndrome Williams syndrome is a genetic disorder characterized by mild , distinctive facial appearance, problems with calcium balance, and blood vessel disease. http://adam.about.com/encyclopedia/001116trt.htm?terms=affinity+health+care   adam.about.com - summary Williams syndrome - References - Genetics Home Reference The neurobiology of Williams syndrome: cascading influences of visual system impairment? ... Gene Review: Williams Syndrome. Mervis CB, Becerra AM. Language ... http://ghr.nlm.nih.gov/condition=williamssyndrome/show/References   ghr.nlm.nih.gov - summary Zori Stalker Williams syndrome - Wikipedia, the free encyclopedia Zori Stalker Williams syndrome has an autosomal dominant pattern of inheritance. ... Zori Stalker Williams syndrome at NIH's Office of Rare Diseases ... http://en.wikipedia.org/wiki/Zori_Stalker_Williams_syndrome   en.wikipedia.org - summary Coeliac disease in Williams syndrome. CD has also been found in sporadic Williams syndrome (WS) patients. ... Williams Syndrome/blood. Williams Syndrome/complications. Williams Syndrome/pathology ... http://www.ncbi.nlm.nih.gov/pubmed/11694549?dopt=Abstract   www.ncbi.nlm.nih.gov - summary WILLIAMS SYNDROME - Pedbase.org the recognition of Williams Syndrome (WS) arose from the identification of two ... syndrome first described by Williams et al. in 1961 ... http://pedbase.org/w/williams-syndrome   pedbase.org - summary Prevalence estimation of Williams syndrome. There are limited population-based data on the occurrence of Williams syndrome. ... We also conclude that Williams syndrome is not an uncommon cause of mental ... http://www.ncbi.nlm.nih.gov/pubmed/12088082   www.ncbi.nlm.nih.gov - summary Williams syndrome: a genetic deletion disorder presenting clues to the ... Williams syndrome is a neurodevelopmental disorder that results from the ... Williams syndrome has enormous heuristic value because its pathological feature ... http://www.ncbi.nlm.nih.gov/pubmed/18163035   www.ncbi.nlm.nih.gov - summary [History of Williams syndrome] History of the Williams syndrome (WS) represents a process of detailed analysis ... Williams Syndrome/genetics. Williams Syndrome/history ... http://www.ncbi.nlm.nih.gov/pubmed/12515042   www.ncbi.nlm.nih.gov - summary A novel human gene, WSTF, is deleted in Williams syndrome. ... human gene, WSTF, is deleted in Williams syndrome. Lu X, Meng X, Morris CA, ... Williams syndrome (WS) is a developmental disorder caused by deletion of ... http://www.ncbi.nlm.nih.gov/pubmed/9828126   www.ncbi.nlm.nih.gov - summary Williams Syndrome Important It is possible that the main title of the report Williams Syndrome is not the name you expected. ... http://www.webmd.com/children/Williams-Syndrome-11011   www.webmd.com - summary Hypercalcemia: Metabolic, Electrolyte, and Toxic Disorders in Neonates ... Williams syndrome includes supravalvular aortic stenosis, an elfin facies, and ... diagnosis of exclusion and is difficult to differentiate from Williams syndrome. ... http://www.merck.com/mmpe/print/sec19/ch274/ch274c.html   www.merck.com - summary Cardiovascular manifestations in 75 patients with Williams syndrome. ... assessed in a population of 75 Williams syndrome (WS) patients aged 4 months to ... Williams Syndrome/genetics. Substances: Elastin. PMID: 12161592 [PubMed ... http://www.ncbi.nlm.nih.gov/pubmed/12161592?ordinalpos=34&it...   www.ncbi.nlm.nih.gov - summary Williams Syndrome (WMS, WS) National Library of Medicine provides a list of synonyms, a summary of the syndrome, and major physical features. http://www.nlm.nih.gov/archive/20061212/mesh/jablonski/cgi/j...   www.nlm.nih.gov - summary Talk:Williams syndrome - Wikipedia, the free encyclopedia edit · history · watch · refresh To-do list for Williams syndrome: ... Missing are links to the Williams Syndrome Associations in the UK, Canada, ... http://en.wikipedia.org/wiki/Talk:Williams_syndrome   en.wikipedia.org - summary ELN - elastin - Genetics Home Reference Williams syndrome - associated with the ELN gene ... in a region of chromosome 7 that is deleted in people with Williams syndrome. ... http://ghr.nlm.nih.gov/gene=eln   ghr.nlm.nih.gov - summary WebMD Health A-Z - Find reliable health and medical information on ... Find a comprehensive index of trusted health and medical information. It is your ultimate guide to reliable health ... Syndrome. WMS -- Williams Syndrome ... http://www.webmd.com/a-to-z-guides/health-topics/wk-wo.htm   www.webmd.com - summary Williams syndrome transcription factor (LOC398269) African clawed frog protein-coding gene LOC398269. Represented by 23 ESTs from 9 ... Xenopus laevis Williams syndrome transcription factor mRNA, partial cds. PA ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Xl&CID=16009   www.ncbi.nlm.nih.gov - summary MedlinePlus Medical Encyclopedia: Topics beginning with W Wermer syndrome see Multiple endocrine neoplasia (MEN) I ... Williams-Beuren syndrome see Williams syndrome. Williams syndrome ... http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_W.htm   www.nlm.nih.gov - summary Risk of sudden death in the Williams-Beuren syndrome. Williams-Beuren syndrome (WBS) is a genetic disorder characterized by a ... Risk Factors. Williams Syndrome/mortality* PMID: 15150772 [PubMed - indexed for MEDLINE] ... http://www.ncbi.nlm.nih.gov/pubmed/15150772?dopt=Abstract   www.ncbi.nlm.nih.gov - summary Williams-Campbell syndrome - Wikipedia, the free encyclopedia Williams-Campbell syndrome is a disease of the airways where cartilage in the ... Lung Transplantation for Williams-Campbell Syndrome" ... http://en.wikipedia.org/wiki/Williams-Campbell_syndrome   en.wikipedia.org - summary GTF2I - References - Genetics Home Reference Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and ... Neural mechanisms in Williams syndrome: a unique window to genetic influences on ... http://ghr.nlm.nih.gov/gene=gtf2i/show/References   ghr.nlm.nih.gov - summary Cushing's Syndrome-Topic Overview Cushing's syndrome is a rare disorder that develops when the body ... Robin Williams. 5. Why Eat Fatty Fish. 6. Circumcision Benefit. 7. Pancreatic Cancer. 8 ... http://www.webmd.com/a-to-z-guides/cushings-syndrome-topic-overview?page=2   www.webmd.com - summary Health Information A member of SSM Health Care. Body, Mind, Spirit... We care for the whole person. ... Williams syndrome. Williams-Beuren syndrome. Wilms tumor. Wilson's disease ... http://ssmhealth.adam.com/content.aspx?pid=1&gid=200000&sub=Disease&alpha=W   ssmhealth.adam.com - summary Index: WI: Merck Manual Professional Williams-Campbell syndrome. Factors Predisposing to Bronchiectasis. Williams syndrome. Aortic Stenosis: Etiology and Pathophysiology ... http://www.merck.com/mmpe/index/ind_wi.html   www.merck.com - summary Bones, muscles, and connective tissues - Genetics Home Reference Hypercalcemia-Supravalvar Aortic Stenosis see Williams syndrome ... Infantile hypercalcemia see Williams syndrome ... stenosis syndrome see Williams syndrome ... http://ghr.nlm.nih.gov/ghr/conditionsByCategory/show/bonesmu...   ghr.nlm.nih.gov - summary Montel Williams: Living with MS Montel Williams faces challenges everyday in his role as ... Multiple Sclerosis: Montel Williams and MS Related Articles. Devic's Syndrome. New on MedicineNet ... http://www.medicinenet.com/script/main/art.asp?articlekey=53785&page=2   www.medicinenet.com - summary J. C. P. Williams - Wikipedia, the free encyclopedia ... called Williams Syndrome in 1961, while working as the Registrar at Greenlane ... In the wake of his discovery, Williams was offered a position at the Mayo ... http://en.wikipedia.org/wiki/J._C._P._Williams   en.wikipedia.org - summary Brain and nervous system - Genetics Home Reference ... Aortic Stenosis see Williams syndrome ... see Williams syndrome ... WS see Williams syndrome. X-ALD see X-linked adrenoleukodystrophy. X-linked ... http://ghr.nlm.nih.gov/ghr/conditionsByCategory/show/brainandnervoussystem   ghr.nlm.nih.gov - summary MedlinePlus Medical Encyclopedia: Short stature Down syndrome. Hypothyroidism that develops before birth ... Russell-Silver syndrome. Turner syndrome. Williams syndrome. This list is not all-inclusive. ... http://www.nlm.nih.gov/medlineplus/ency/article/003271.htm   www.nlm.nih.gov - summary Disease Reference Waterhouse-Friderichsen syndrome. Wax blockage. Weak bones - premature infants ... Williams syndrome. Williams-Beuren syndrome. Wilms tumor. Wilson's disease ... http://adam.about.com/HIE/diseidxw.htm   adam.about.com - summary Do faces capture the attention of individuals with Williams syndrome or ... Do faces capture the attention of individuals with Williams syndrome or autism? ... neuro-developmental disorders of Williams syndrome (WS) and autism can reveal ... http://www.ncbi.nlm.nih.gov/pubmed/18787936?ordinalpos=3&ito...   www.ncbi.nlm.nih.gov - summary : Mercy Adam Content : Williams syndrome. Williams-Beuren syndrome. Willow-leaved foxglove poisoning. Wilms tumor ... Wolff-Parkinson-White syndrome. Women and heart disease ... http://mercycanton3.adam.com/content.aspx?productId=101&alpha=W   mercycanton3.adam.com - summary A novel human gene FKBP6 is deleted in Williams syndrome. ... human gene FKBP6 is deleted in Williams syndrome. Meng X, Lu X, Morris CA, ... Williams syndrome (WS) is a developmental disorder caused by haploinsufficiency ... http://www.ncbi.nlm.nih.gov/pubmed/9782077   www.ncbi.nlm.nih.gov - summary [William's syndrome] William's syndrome is of great interest to neurosclence as it is expected to ... Although patients with this syndrome have moderate levels of learning disability, ... http://www.ncbi.nlm.nih.gov/pubmed/18069600   www.ncbi.nlm.nih.gov - summary Heart and circulation - Genetics Home Reference Hypercalcemia-Supravalvar Aortic Stenosis see Williams syndrome. hypercholesterolemia ... Infantile hypercalcemia see Williams syndrome ... http://ghr.nlm.nih.gov/conditionCategory=heartandcirculation   ghr.nlm.nih.gov - summary Chromosomal Deletion Syndromes: Chromosomal Anomalies: Merck Manual ... 5p-Deletion (cri du chat syndrome) ... Prader-Willi syndrome (see Endocrine and Metabolic Disorders in Children: Secondary) ... Williams syndrome. 7q11.23 ... http://www.merck.com/mmpe/print/sec19/ch294/ch294f.html   www.merck.com - summary Asperger's Syndrome-References A reference list about Asperger's syndrome. ... Philadelphia: Lippincott Williams and Wilkins. WebMD Medical Reference from Healthwise ... http://www.webmd.com/brain/autism/tc/aspergers-syndrome-references   www.webmd.com - summary LIMK1 - References - Genetics Home Reference ... Williams ... 115: linking cytoskeletal defects to Williams syndrome. Bioessays. ... Tassabehji M. Williams-Beuren syndrome: a challenge for genotype ... http://ghr.nlm.nih.gov/gene=limk1/show/References   ghr.nlm.nih.gov - summary Early development in Williams syndrome. Early development in Williams syndrome. Tsai SW, Wu SK, Liou YM, Shu SG. ... Juvenile Williams syndrome patients were apparently retarded (<10 per thousand ... http://www.ncbi.nlm.nih.gov/pubmed/18353064   www.ncbi.nlm.nih.gov - summary Neurologic Diseases - Genetics Home Reference Menkes syndrome. metachromatic leukodystrophy ... Williams syndrome. Wilson disease. X-linked adrenoleukodystrophy. X-linked dystonia-parkinsonism ... http://ghr.nlm.nih.gov/medlineplusTopic=neurologicdiseases   ghr.nlm.nih.gov - summary GTF2IRD1 - GTF2I repeat domain containing 1 - Genetics Home Reference Williams syndrome - associated with the GTF2IRD1 gene ... in a region of chromosome 7 that is deleted in people with Williams syndrome. ... http://ghr.nlm.nih.gov/search/term=12239342?area=pubmed-id   ghr.nlm.nih.gov - summary show more 1  2