NARRATOR 1: In the year 2194‚ in Harare‚ the sprawling capital of Zimbabwe‚ there is a special place called Resthaven. NARRATOR 2: Surrounded by a huge wall that keeps out the city‚ the people of Resthaven choose to live as Africans lived for thousands of years—in small tribal villages‚ raising their own food‚ and following the ancient traditions. NARRATOR 1: Into this haven stumble three children of a high government security officer—the boy Tendai‚ his younger sister Rita‚ and their little
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Having a Down syndrome is such a difficult situation for an individual to have. They have slow physical and mental capabilities that lead them to discrimination. Physical features of having a Down syndrome. Including flattening of the head; slanting of the eyelids; a gap between the first and the second toes; a depressed nasal bridge; relatively small ears‚ mouth‚ hands and feet; short stature; decreased muscle tone and loose ligaments among others. Not every child with Down syndrome has all of these
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Infant Neurosensory Development Brain Development In Infants Trident Technical College September 11‚ 2013 In the article‚ Infant Neurosensory Development: Considerations for Infant Child Care‚ The internal and external environments affect the development of physical and neural structures that guide visual‚ auditory‚ chemosensory‚ somatosensory‚ and limbic system functions. These systems both contribute and respond to cognitive development‚ including memory (Fields2005)
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The Demise Of The Death Penalty Mandy Szwedko Western Governors University WGU Student ID # 000383758 Thesis Statement: Research suggests that capital punishment should be abolished to obviate mishandled executions‚ prevent wrongfully convicted citizens from being put to death and to lower taxpayer dollars for incurred expenses for inmates on death row. Annotated Bibliography Capital punishment‚ known as the death penalty is punishment by death and is reserved for the most heinous of
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Down syndrome Down syndrome is one of the most common genetic disorders‚ occurring one in every 600 births (Davis‚ 2008). 3‚500-5‚000 children are born with Down syndrome every year in the United States alone (Pueschel‚ 2008). Down syndrome or mongolism was first identified by John Langdon Down in 1866 although the syndrome has been around for many centuries. In fact‚ according to many paintings dated back to the sixteenth century show pictures of children with Down syndrome like features (Carr
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Marfan Syndrome Have you ever wondered about the diseases that you can get from your parents? One of these major diseases that can change someone’s life is called the Marfan Syndrome. Marfan Syndrome is a disorder of connective tissue that is inherited from the parents. The bones and circulatory system are usually the parts of the body that are longer and the ones that are changed because of the disease. There are many things that can cause a disease. Marfan syndrome is caused by a mutation
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Williams syndrome also recognized as Williams-Beuren syndrome is a genetic disorder caused by a deletion of more than twenty five genes from chromosome 7. Although Williams syndrome is often non-hereditary‚ the chances of the syndrome being passed on if an individual with Williams syndrome has a child are fifty percent. Individuals born with Williams syndrome often possess distinctive facial features which make the syndrome easily recognized. These features include wide spaces between their teeth
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Inside Rett Syndrome Christina Wenn April 10‚ 2013 Rett syndrome is a genetic disorder that I have dealt with first-hand. I babysat a set of twins in my neighborhood‚ and one of the twins‚ Morgan‚ was diagnosed with Rett syndrome as an infant. I started babysitting the twins‚ Morgan and Ryan‚ when I was a freshman in high school‚ but I mainly took care of Morgan. She would giggle and smile‚ but other than that she was mute. Morgan ate baby food and watched Disney movies. She also wore a diaper
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Turner Syndrome It was first described in 1930‚ and first diagnose in 1959. Now a days‚ 1 of 2‚000 females are born with this syndrome. Turner syndrome (also known as TS) is named after the famous endocrinologist Henry Turner‚ who was the first person to described and published any findings about this syndrome. This condition is also known as Bonnevie-Ullrich syndrome‚ Gonadal dysgenesis‚ and Monosomy X. The syndrome is a non-inherited chromosomal condition that only occurs in females. It’s cause
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conducted around the topics of crush syndrome and amputation‚ which depending on the severity of the crush can coincide with one another. This paper will discuss various medical aspects‚ treatment‚ assessment‚ psychosocial/psychological issues and some research data pertaining earthquakes related to amputation and crush syndrome. Crush injuries can occur through the means of a natural disaster‚ acts of war‚ traffic collisions‚ as well as industrial accidents. Crush syndrome differs from a crush injury depending
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