關於 william syndrome ，我們在網路上蒐集到這些相關的討論、資訊與評價

#11. Williams syndrome - Genetic and Rare Diseases Information ...

A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Williams syndrome.

#12. Williams Syndrome: Symptoms, Diagnosis, and Treatments

What is Williams syndrome? Williams syndrome, also called Williams-Beuren syndrome, is a rare genetic disorder. It causes many developmental problems.

#13. Williams Syndrome - an overview | ScienceDirect Topics

William's Syndrome (WS) is a neurodevelopmental genetic disorder which occurs in about 1 in 20 000 live births. There are a number of clinical features, but of ...

#14. Williams syndrome - UpToDate

Williams syndrome (WS, OMIM #194050 [1]), also known as Williams-Beuren syndrome, is a multisystem, contiguous gene deletion syndrome caused ...

#15. 194050 - WILLIAMS-BEUREN SYNDROME; WBS - OMIM

Williams -Beuren syndrome is a multisystem disorder caused by hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23, which contains approximately 28 ...

#16. Williams syndrome: diagnosis & support - Raising Children ...

Williams syndrome is a rare condition that happens in 1 in 7500-10 000 births. This syndrome is sometimes known as Williams-Beuren syndrome. It was first ...

#17. Williams syndrome | Radiology Reference Article - Radiopaedia

Williams syndrome (WS), sometimes called Williams-Beuren syndrome, is characterized by some or all of the following features: craniofacial ...

#18. Williams Syndrome: Background, Pathophysiology, Etiology

Originally described independently by Williams and Beuren in 1961, Williams syndrome (WS) is a rare genetic condition.

#19. Williams Syndrome | Mencap

People with Williams syndrome can develop physical and mental health problems later in life, including anxiety and depression. People with Williams syndrome are ...

#20. Williams Syndrome Explained

Williams Syndrome is a rare congenital disorder that occurs randomly and affects around one in 18,000 people in the UK. It is non-hereditary and causes ...

#21. Williams Syndrome | Boston Children's Hospital

Williams syndrome is a rare (affecting 1 in 10,000 people) developmental disorder that can affect many parts of the body, including the heart and blood ...

#22. Williams Syndrome Symptoms, Signs, Treatment & Life ...

Williams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual disability ...

#23. Williams Syndrome - Developmental and Behavioral Pediatrics

Williams syndrome is a genetic condition in which there is a small deletion of material on chromosome 7 (7q11.23 microdeletion). It is present at birth and ...

#24. Living with Williams Syndrome (A Condition that Makes You ...

#25. Williams syndrome | Nature Reviews Disease Primers

Williams syndrome (WS) is a relatively rare microdeletion disorder that occurs in as many as 1:7,500 individuals.

#26. Williams Syndrome - Stanford Children's Health

Williams syndrome is a genetic condition that affects many parts of the body. The condition is caused by missing genes from chromosome No. 7 that are ...

#27. Williams syndrome - Orphanet

A rare genetic multisystemic neurodevelopmental disorder characterized by a distinct facial appearance, cardiac anomalies (most frequently supravalvular aortic ...

#28. Williams syndrome - Healthdirect Australia

Williams syndrome is a genetic condition present from birth that occurs because a small piece of chromosome 7 does not form properly after conception.

#29. Williams Syndrome, Human Self-Domestication ... - Frontiers

One source of these changes might be human self-domestication. Williams syndrome (WS) is a clinical condition with a clearly defined genetic ...

#30. William's Syndrome - Physiopedia

William's Syndrome is a result of a spontaneous microdeletion of a band on chromosome 7. ... The deletion can be inherited from either the mother or father of a ...

#31. Williams Syndrome - American Association for Pediatric ...

Williams Syndrome is a rare disorder caused by a deletion of genetic material from a specific region of chromosome 7 that affects an elastin ...

#32. Williams Syndrome - St. Louis Children's Hospital

Williams syndrome is caused by 26-28 missing genes in a small region on one of the child's chromosomes. In most cases, the child with Williams syndrome is the ...

#33. Williams Syndrome - BrainFacts.org

Williams Syndrome (WS) is a rare genetic disorder characterized by mild to moderate delays in cognitive development or learning difficulties, a distinctive ...

#34. Williams-Beuren Syndrome: Genes and Mechanisms

Abstract. Williams-Beuren syndrome (WBS; OMIM 194050) is caused by heterozygous deletions of ∼1.6 Mb of chromosomal sub-band 7q11.23.

#35. Williams syndrome: an update on clinical and molecular aspects

Williams syndrome is a neurodevelopmental disorder associated with a characteristic physical and behavioural phenotype. The syndrome was described in 1961 ...

#36. Oral Findings and Dental Treatment in a Child with Williams ...

Williams-Beuren syndrome (WBS), also known as Williams syndrome, is a rare congenital disorder involving cardiovascular problems, mental retardation, ...

#37. Williams Syndrome Clinic | The Children's Hospital at Montefiore

Williams syndrome (WS) is a rare genetic condition affecting growth, physical health, and learning abilities. A deletion of around 25 genes on chromosome ...

#38. Williams syndrome Information | Mount Sinai - New York

Williams syndrome is caused by not having a copy of 25 to 27 genes on chromosome number 7. ... One of the missing genes is the gene that produces elastin. This is ...

#39. Williams Syndrome - Center for Interdisciplinary Brain ...

What is Williams Syndrome? · Impaired visuospatial abilities with preserved facial processing · Impaired problem solving · Preserved language abilities · Love of ...

#40. Williams Syndrome Clinic - Nationwide Children's Hospital

The Williams Syndrome Clinic provides treatment and support services to children with Williams syndrome and their families.

#41. Williams Syndrome: A Case Series - Indian Pediatrics

It is characterized by cardiovascular disease, distinctive facies and personality, mild intellectual disability, unique personality, and connective tissue ...

#42. What is Williams Syndrome?

Williams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual ...

#43. Health Care Supervision for Children With Williams Syndrome

for children with Williams syndrome (WS) who were diagnosed by using clinical features and with chromosome 7 microdeletion confirmed by.

#44. Williams syndrome Definition & Meaning - Merriam-Webster

The meaning of Williams syndrome is a rare genetic disorder marked especially by hypercalcemia of infants, heart defects, characteristic facial ...

#45. Williams syndrome | Spectrum | Autism Research News

Children with Williams syndrome have a range of cognitive symptoms, including a happy and highly social demeanor, developmental delay and strong language skills ...

#46. Cardiovascular Disease in Williams Syndrome | Circulation

Williams syndrome (WS), also referred to as Williams-Beuren syndrome (Online Mendelian Inheritance in Man 194050), is a congenital, ...

#47. Analysis of Cerebral Shape in Williams Syndrome - JAMA ...

BackgroundAs a neurobehavioral disorder with a specific neurocognitive profile and a well-defined genetic etiology, Williams syndrome (WMS) provides an ...

#48. Learning Disabilities and other challenges | Williams Syndrome

Williams syndrome is a lifelong condition; it cannot be cured. It causes learning disabilities, certain distinctive facial features, and an increased likelihood ...

#49. Considerations for dental treatment of Williams syndrome ...

Williams syndrome is a rare congenital disorder with various physical abnormalities and characterized by facial, oral, and dental features.

#50. 威廉氏症候群（Williams syndrome, WS; 7q11.23deletion）

威廉氏症候群（Williams syndrome, WS; 7q11.23deletion）. 彙整者：莊雅琴臨床心理師. 撰文日期：2018/2/23. 臨床表徵(Clinical Characteristics)：. 症狀類別.

#51. Williams Syndrome

23. According to the Williams Syndrome Association, children with Williams Syndrome are characterized by "[S]mall upturned nose, long philtrum (upper lip length) ...

#52. Fat Distribution and Glucose Metabolism in Williams Syndrome

Williams Syndrome (WS) is a genetic syndrome with features that may include vascular stenoses, neuro-developmental changes, and a variety of ...

#53. Williams Syndrome Pictures, Signs, Symptoms, Causes & Life ...

Williams syndrome (also termed Williams-Beuren syndrome) is a rare genetic disorder (in chromosome 7) that results in prenatal and postnatal growth disorder, ...

#54. Williams syndrom - Socialstyrelsen

Health care supervision for children with Williams syndrome. Pediatrics 2001; 107: 1192-1204. Asada K, Ikatura S. Social phenotypes of autism ...

#55. Health Care Supervision for Children With Williams Syndrome

Williams syndrome (WS), also known as Williams-Beuren syndrome, is caused by a deletion of part of chromosome 7 and is a multisystem disorder ...

#56. Williams Syndrome - Cancer Therapy Advisor

Williams syndrome (WS) is a disorder caused by a microdeletion on chromosome 7 which leads to characteristic facial features, heart disease (supravalvular ...

#57. Williams-Beuren Syndrome - Symptoms, Diagnosis, Treatment

Williams syndrome is a rare genetic disorder that affects many parts of the body. This condition usually presents at birth and is ...

#58. A Life Without Fear: Dealing With Williams Syndrome - NPR

Can I go home with you?" Jessica heard Isabelle plead. Driven To Trust. Jessica's daughter, Isabelle, has Williams syndrome, a genetic disorder ...

#59. Ophthalmic Manifestations of Williams Syndrome | IOVS

Purpose : Williams syndrome (WS) is an inherited disorder caused by microdeletions of chromosome 7q11.23, including ELN. Hemizygosity for the ELN gene ...

#60. Evaluating quality of life in families with Williams Syndrome ...

Williams Syndrome is a developmental disorder characterized by a variable intellectual disability. People with Williams Syndrome need the ...

#61. Williams–Beuren Syndrome | NEJM

Williams –Beuren syndrome, a multisystem disorder caused by the deletion of a chromosome region of 1.5 million to 1.8 million base pairs ...

#62. Williams syndrome and hyperacusis. - Dizziness-and-balance ...

Williams syndrome (WS)is a genetic disorder that has, among other symptoms, hyperacusis (phonophobia), anxiety, and abnormal cortical ...

#63. Living with Williams Syndrome, the 'opposite of autism' - BBC

Chris has Williams Syndrome (WS), a rare genetic disorder affecting around one in 18,000 people in Britain. It has often been dubbed the ...

#64. Williams Syndrome Associated With Autism Spectrum Disorder

Williams-Beuren syndrome, or simply Williams syndrome (WS), is a rare chromosomal abnormality with an incidence rate of one out of 20,000 live ...

#65. Williams Syndrome and 15q Duplication: Coincidence versus ...

Williams syndrome is a multisystem disorder caused by contiguous gene deletion in 7q11.23, commonly associated with distinctive facial ...

#66. Williams Syndrome and Related Disorders - Annual Reviews

Williams syndrome (WS), a multisystem disorder that occurs in 1/20,000 births, is caused by a ∼1.5 Mb deletion encompassing the elastin gene [ELN] at ...

#67. Williams Syndrome across Languages - John Benjamins ...

Williams Syndrome (WS), aka Williams Beuren Syndrome, is a developmental disorder that we have known about for some forty years.

#68. Hypertension and Williams Syndrome: Harold's Story

People with Williams syndrome have a cluster of characteristics, including distinctive facial features; outgoing, engaging personalities (often ...

#69. Williams-Beuren Syndrome (WBS) - MalaCards

Attention deficit disorder (ADD), problems with anxiety, and phobias are common among people with this disorder.Young children with Williams syndrome have ...

#70. A case of Williams syndrome with suspected coexisting ...

A case of Williams syndrome with suspected coexisting ectopic aldosterone-producing tumor in the liver · Background · Case presentation.

#71. Echocardiographic and Doppler findings in the Williams ...

Williams syndrome is a relatively rare, usually nonfamilial disorder, characterized by typical facial features, growth deficiency, mental retardation, ...

#72. Williams Syndrome and the Brain - Scientific American

Williams Syndrome and the Brain. To gain fresh insights into how the brain is organized, investigators are turning to a little known disorder.

#73. William Syndrome - Zero To Finals

William syndrome is caused by a deletion of genetic material on one copy of chromosome 7, resulting in the person only having a single copy of the genes on ...

#74. Explainer: what is Williams syndrome? - The Conversation

Let's deal with the differences first. A striking feature of Williams syndrome is high sociability and empathy for others, which is very ...

#75. Prevalence Estimation of Williams Syndrome - SAGE Journals

The epidemiologic study revealed three children with Williams syndrome, whereas one additional case complying with our demographic criteria was identified in ...

#76. Williams Syndrome, Pediatric Cardiac Center Florida | Nemours

Williams syndrome is a rare genetic disorder that affects the physical development of multiple body functions — particularly the heart and circulatory ...

#77. The Effect of Individual Differences Across the Life Span

This research aimed to comprehensively explore psychopathology in Williams syndrome (WS) across the life span and evaluate the relationship ...

#78. Williams Syndrome Resources | Florida Department of Health

The Williams Syndrome Association's (WSA) mission is to advance the interests of all individuals with Williams syndrome throughout their ...

#79. Williams syndrome — Department of Psychological and Brain ...

A large proportion of children and adolescents with Williams syndrome have attention deficit hyperactivity disorder (ADHD); some have inattention and others ...

#80. Williams Syndrome: Neuropsychological Findings and ...

Williams syndrome (WS) is a genetic disorder resulting from a deletion on Chromosome 7. Individuals with WS exhibit distinct physical features such as faci.

#81. Hyperacusis in Williams syndrome | Neurology

Conclusions: Hyperacusis in Williams syndrome (WS) is associated with a high-frequency hearing loss resembling the configuration of noise- ...

#82. Williams syndrome | Osmosis

Williams syndrome, also known as Williams-Beuren syndrome, is named after Dr. J. C. P. Williams who first described it. This is a chromosome disorder in which a ...

#83. Williams Syndrome | National Council for Special Education

This is a rare congenital disorder of chromosome 7. It is diagnosed with a blood test and often can go undiagnosed for a long time.

#84. Williams syndrome

Definition. Williams syndrome is a rare disorder that can lead to problems with development. · Alternative Names. Williams-Beuren syndrome; WBS; ...

#85. Williams syndrome, the brain, and music - Salk Institute

Identified more than 40 years ago, Williams syndrome arises from a faulty recombination event during the development of sperm or egg cells. As a ...

#86. Description of common musculoskeletal findings in Williams ...

PDF | Williams syndrome (WS), also referred to as Williams-Beuren syndrome (WBS), is a relatively rare genetic disorder affecting ∼1/10000 ...

#87. Williams syndrome • LITFL • Medical Eponym Library

Williams -Beuren syndrome: Generalized disorder characterized by unusual facies, abnormal behavioral abilities, cardiovascular anomalies, ...

#88. WS7F Williams Syndrome, 7q11.23 Deletion, FISH, Varies

WS7F : Williams syndrome (WS) is a genetic disorder that occurs in 1/20000 to 1/50000 live births. Although WS is typically a sporadic disorder, ...

#89. Williams–Beuren syndrome: a complete guide for oral ...

Introduction: Williams–Beuren syndrome is a rare, congenital, multisystem disorder, resulting from genetic alterations on chromosome 7q11.23 ...

#90. Williams syndrome - Trait Document | My46

Williams syndrome is a multi-system genetic disorder with both medical and developmental features. A hallmark medical feature of Williams syndrome is blood ...

#91. Williams-Beuren's Syndrome: A Case Report - Hindawi

It is characterized by congenital heart defects (CHD), skeletal and renal anomalies, cognitive disorder, social personality disorder and dysmorphic facies. We ...

#92. Celiac Disease and Williams Syndrome | BeyondCeliac.org

Williams syndrome is a genetic condition that occurs when a person is missing part of the genetic material of chromosome 7. This condition is present at birth ...

#93. A Clue to Human 'Self-Domestication': Williams Syndrome

People with Williams syndrome lack 26 to 28 neighboring genes on the seventh human chromosome. This region includes various genes with diverse ...

#94. Children With Williams Syndrome: Language, Cognitive, and ...

Williams syndrome (WS) is a rare genetic disorder characterized by heart disease, failure to thrive, hearing loss, intellectual or learning ...

#95. New Zealand Williams Syndrome Association - Home

Williams syndrome (WS) is a genetic condition that is present at birth and can affect anyone. It is characterized by medical problems, ...

#96. Neuroscientists reverse some behavioral symptoms of ...

Williams Syndrome, a rare neurodevelopmental disorder that affects about 1 in 10,000 babies born in the United States, produces a range of ...

#97. Williams Syndrome: The extent of agreement between parent ...

Williams syndrome (WS) is a rare genetic disorder (1 in 7,500 to 1 in 20,000 live births 1,2 ) caused by a microdeletion at 7q11.23. The effects include facial ...

#98. How a Real Genetic Disorder Could Have Inspired Fairy Tales

Many people go their whole lives without meeting someone who has Williams syndrome. But for those of us who do, the experience can feel ...