Williams syndrome facial

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The characteristic facial features include puffiness around the eyes, short nose, wide mouth, full lips, full cheeks and a small chin. They can have a short stature, sloping shoulders, long neck and limited movement in their joints. They also have strong verbal abilities, highly social personalities, and a love for music. Williams Syndrome is a rare disorder caused by a deletion of genetic material from a specific region of chromosome 7 that affects an elastin gene. Elastin is a protein that gives blood vessels strength and the ability to stretch.
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Williams syndrome: What you need to know

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Williams syndrome: Features, causes, and treatment

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. People with Williams syndrome typically have difficulty with visual-spatial tasks such as drawing and assembling puzzles, but they tend to do well on tasks that involve spoken language, music, and learning by repetition rote memorization. Affected individuals have outgoing, engaging personalities and tend to take an extreme interest in other people.
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Williams syndrome

Williams syndrome is a rare neurodevelopmental genetic disorder that features mild learning or developmental challenges, a high levels of calcium in the blood and urine, and a markedly outgoing personality. Unique personality traits include a high level of sociability and very good communication skills. The high level of verbal skills may mask other developmental problems and sometimes contribute towards a late diagnosis.
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Williams syndrome is a rare genetic condition. It is characterised by distinctive physical features and behaviours, including a distinctive facial appearance, mild intellectual disability and an overly sociable personality. Williams syndrome is caused by a missing segment a 'deletion' of genetic material on chromosome 7. These deletions occur randomly. About one in every 20, babies is born with Williams syndrome.
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