Williams syndrome facial

Treatment, prognosis, and life-expectancy for a person with congestive heart failure depends upon the stage of the disease. Williams syndrome is a developmental disorder that affects many parts of the body. Williams syndrome may cause poor growth in childhood, and most adults with the condition are shorter than average. Leprechaunism is a rare progressive inherited endocrine disorder characterized by overgrowth hyperplasia of the pancreas, inability to properly utilize insulin insulin resistance , and excessive amounts of estrogen. In contrast, fine motor skills often lag behind their IQ-matched peers, and, the sense of spatial relationships is very poor. Eye crossing Difficulty with potty training, increased frequency with which the child needs to go or urgency leading to accidents or the feeling of pain with urination Hernias and other problems of connective tissue such as loose or tight joints or scoliosis What causes Williams Syndrome?
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Introduction

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American Association for Pediatric Ophthalmology and Strabismus

Handbook of neurodevelopmental and genetic disorders in children. Musculoskeletal abnormalities associated with Williams syndrome may include depression of the breastbone pectus excavatum , abnormal side-to-side or front-to-back curvature of the spine scoliosis or kyphosis , or an awkward gait. The definition of a genetic disease is a disorder or condition caused by abnormalities in a person's genome. Diagnosis and treatment of chest pain depends upon the cause and clinical presentation of the patient's chest pain. Some affected individuals may have visual difficulties; they may tend to view a picture in parts as opposed to seeing it as a whole. Social cognition in Williams syndrome.
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Williams Syndrome — AAPOS

Journal of Child Psychology and Psychiatry, 39, Language and communication in autism. There is no standard treatment protocol. Developmental Science, 5, For more information, contact: It is, nevertheless, important to make a distinction here between constraints on the process of social cognitive development and confounding factors that might constrain performance on measures of social cognitive functioning. Typically, there is narrowing in the aorta producing supravalvular aortic stenosis SVAS , or narrowing in the pulmonary arteries.
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Such characteristic facial features may include a round face, full cheeks, thick lips, a large mouth that is usually held open, and a broad nasal bridge with nostrils that flare forward anteverted nares. Every child with Williams syndrome is different. Noonan syndrome is a rare genetic disorder that is typically evident at birth congenital. Attention Deficit Hyperactivity disorder is a behavioral disorder of childhood characterized by a short attention span, excessive impulsiveness, and inappropriate hyperactivity. Comparisons may be useful for a differential diagnosis:
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