Facial features of williams syndrome

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Williams syndrome, also known as Williams-Beuren syndrome, is a rare genetic disorder characterized by growth delays before and after birth (prenatal and postnatal growth retardation), short stature, a varying degree of mental deficiency, and distinctive facial features that typically become more pronounced with age. Williams syndrome is a rare and genetic disorder that is responsible for neurodevelopmental abnormalities and distinct facial features like an elf. Elastin is a protein that enables the blood vessels in the body as well as other tissues to stretch.

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Williams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual disability or learning problems, unique personality characteristics, distinctive facial features, and heart and blood vessel (cardiovascular) problems. Williams syndrome, also known as Williams-Beuren syndrome (WBS), results from microdeletion in a small region of chromosome 7. The deleted region includes 26 to 28 genes, and researchers believe that a loss of several of these genes probably contributes to the characteristic features of this disorder.

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Williams syndrome is a rare genetic disorder that causes a variety of symptoms and learning issues. Children with this syndrome could have problems with their heart, blood vessels, kidneys, and. 2 The syndrome is characterized by mental retardation or moderate learning difficulties, distinctive facial features, attention deficit disorder, and a unique personality combining high levels of anxiety, empathy, and over-friendliness.

Williams syndrome information page

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Dan and I drove home in disbelief and confusion. When we got back to the house, I sat on the couch with Emmy and searched for "Williams syndrome" online. I found images that depicted the facial features that accompany this diagnosis. I poured over the pictures and compared them to my little girl.

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Williams syndrome (WS) is a genetic disorder that affects many parts of the body. Facial features frequently include a broad forehead, short nose and full cheeks, an appearance that has been described as "elfin".

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Williams syndrome (WS) is a rare genetic disorder that occurs in about 1 in 8, births. It is associated with developmental delays and medical problems affecting multiple parts of the body. Features of Williams syndrome include.

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The incidence of Williams syndrome is estimated to be one in 20 live births, and it consists of supravalvular aortic stenosis, characteristic dysmorphic facial features named "elfin face" (wide mouth with long phyltrum and .

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Williams syndrome is a rare genetic condition which can give a person special facial features, a sociable personality, and some learning challenges. Treatment includes vitamin D supplements.

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Williams syndrome is a rare genetic disorder that is caused by the deletion of genetic material on chromosome 7. Typical characteristics include distinctive facial features, mild intellectual disability and an overly sociable personality. Williams syndrome may be undiagnosed, which means that many.

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Specifically, the Williams syndrome, clinically, is characterized by 4 cardinal points: 1) atypical features and facial features, 2) generalized retardation of psychomotor development and specific neurocognitive profile, 3) cardiovascular disorders and 5) possibility [ ].

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Description: Williams syndrome is a form of rare genetic disorder that is characterized by mild to moderate learning difficulties or mental retardation, a unique personality combining high levels of empathy, anxiety, and over-friendliness, and distinctive facial features. Young people with Williams syndrome have small upturned nose, wide mouth, small chin, full lips, long upper lip length, and puffiness around eyes. The facial features become more prominent with age. People with Williams syndrome have complications with heart and blood vessels. Klinefelter syndrome (KS) also known as 47,XXY or XXY, is the set of symptoms that result from two or more X chromosomes in males. The primary features are infertility and small testicles.
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