k Angelman syndrome MODEL RELEASED. Angelman syndrome. 10yearold girl right with Angelman syndrome AS with her siblings. AS is a genetic disorder characterised by arm flapping, excessive laughing even when hurt, a jerky gait and learning problems. It is caused by genes being deleted or inactivated switched off on the copy of chromosome 15 that is inherited from the mother. Roughly one in 15,000 individuals have the condition. Life expectancy is normal, however those with AS are unable to live independently. If the same defect is on the paternal chromosome instead, it causes PraderWilli syndrome. Stock Photo - Afloimages
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Angelman syndrome MODEL RELEASED. Angelman syndrome. 10 year old girl  right  with Angelman syndrome  AS  with her siblings. AS is a genetic disorder characterised by arm flapping, excessive laughing  even when hurt , a jerky gait and learning problems. It is caused by genes being deleted or inactivated  switched off  on the copy of chromosome 15 that is inherited from the mother. Roughly one in 15,000 individuals have the condition. Life expectancy is normal, however those with AS are unable to live independently. If the same defect is on the paternal chromosome instead, it causes Prader Willi syndrome.
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Angelman syndrome

MODEL RELEASED. Angelman syndrome. 10-year-old girl (right) with Angelman syndrome (AS) with her siblings. AS is a genetic disorder characterised by arm flapping, excessive laughing (even when hurt), a jerky gait and learning problems. It is caused by genes being deleted or inactivated (switched off) on the copy of chromosome 15 that is inherited from the mother. Roughly one in 15,000 individuals have the condition. Life expectancy is normal, however those with AS are unable to live independently. If the same defect is on the paternal chromosome instead, it causes Prader-Willi syndrome.

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