...Section A There are certain stereotypes associated with being a middle child in a family. The research that has been done on middle children has allowed scientist to concluded that middle children often associate with feeling neglected, are not motivated, have a negative outlook on life, low-self-esteem, and often feel like they do not belong. The term “middle child syndrome” describes the outcomes that many middle children suffer from. Does being a middle child correlate with negative long-term effects on a child into adulthood? I predict that being a middle child does correlate to negative long-term effects into adulthood. In order to reduce negative outcomes in middle children such as anxiety, depression, and lack of motivation it is important to research to the root of the cause of these negative emotions. Researchers Catherine A. Salmon and Martin Daly study how middle children differ from their siblings in a research article, “Birth Order and Familial Sentiment: Middleborns are Different”. They concluded that birth order did in fact have an effect on a child, especially those who are middleborns. Middleborns are indeed often neglected due to them lacking the uniqueness of being a first or last-born child. Middle children also feel a sense of not being connected to the family, having less parental supervision, and...
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...William has Down syndrome as well as a severe developmental delay. Down syndrome is an extra chromosome that develops when the baby is in their mother’s womb (Evans-Martin, 2009). As Evans-Martin (2009) states children with down syndrome have different physical characteristics compared to a child without down syndrome. For Instance, William joints are looser and he is able to put his feet into his mouth with ease and he tends to lay on the floor with his feet behind his head throughout the day. According to Evan-Martin (2009) William displays the classic features of a child with down syndrome, for instance the middle of his face is flatter than normal and he has a smaller nose which is also flat on the bridge. William has an epicanthal fold...
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...development during adolescence, the most significant aspects of it is the acceptance to her social status, most likely due to her role as a middle child. Although she does not experience an ideal nor typical sixteenth birthday, her continuous treatment as a middle child enables her to remain rational and have reasonable expectations of the unpromising outcome of her birthday. According to Dr. Kevin Lermon’s research, Sam displays typical qualities of a middle child, highlighted most during the interaction with her parents and siblings. Moreover, Sam’s development was shaped from middle child syndrome as her experiences ultimately resulted in her self-esteem issues, and the feeling of inferiority in comparison to her siblings (Danish, 2014). Nonetheless, she carries qualities of being unspoiled, compromising, and most importantly have the deep need to belong. Ultimately, Sam’s role of a middle child enables her to cope easier with her unideal birthday and resolve her inner conflict regarding her social status. Despite the difficulties accompanied by middle child syndrome, Sam does not have other specific factors that affected her development. Sam and her family did not undergo any tragedies that hindered Sam’s development. The most significant aspect of Sam’s adolescence was mostly in part of her experiences as a middle child, specifically middle child syndrome. Throughout 16 Candles, the extent of the character’s development follows a typical pattern in tune to most teenagers during adolescence...
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...delivering a premature child. While pregnant the fetus is very vulnerable to many toxins, such as alcohol, and drugs, so when the mother drinks alcohol, so does the fetus, since blood carries alcohol in the fetus bloodstream. At five weeks the fetus begins to form the brain, which then starts to grow rapidly, this is a crucial time for mothers to nourish their bodies with many proteins and keep away from dangerous toxins. One of the most probable results of drinking while pregnant is the Fetal Alcohol Syndrome (FAS). The Fetal Alcohol Syndrome has been linked to low I.Q. in children. Over the years there has been many studies to determine if a child’s I.Q. if affected by Fetal Alcohol Syndrome. Jones and Smith first introduced Fetal Alcohol Syndrome in the United States in 1973, Jones and Smith described FAS as a “distinctive set of facial anomalies in children whose mothers drank heavily during pregnancy, accompanied by prenatal and/or postnatal growth retardation and cognitive/behavioral problems” (Burden). Children who suffer from FAS commonly have face abnormalities, which may or may not include: flat mid-face, short nose, low nasal bridge, thin lips, short palpable fissures, indistinct philtrum, epicanthal folds, minor ear abnormalities, and micrognathia. These kids also tend to have a much more smaller head than the average child. Fetal Alcohol Syndrome has also been linked to I.Q deficiency. Doctors cannot diagnose a child with AFS without being...
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...Down syndrome was identified as a chromosomal condition in 1959 by a physician. Down Syndrome is a common genetic disorder that people are born with when they have an extra chromosome 21. This could change the health and development of a person. There are at least one in every 700 babies in the United States that are born with this neurological condition. At least 6,000 babies with down syndrome are born each year in the United States. There are different types of down syndrome and different types of effects. People with down syndrome struggle but can do whatever any other person without Down syndrome can do. Down Syndrome is a genetic disorder that includes birth defects. Many people with down syndrome are healthy some need medical care...
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...infant dies unexpectedly of an unknown reason. The unexpected death of a child for an unknown reason, known as Sudden Infant Death Syndrome (SIDS), has impacted many families. SIDS does not affect one race, nationality, or sex it can affect any infant between the ages of 1 month to one year. (Levy Raydo& Reu-Donlon, 2005) Medical professionals should inform expectant parents of all risk factors involved with SIDS, as well as prevention tips as this may drop the percentage rate/heart break of many families. SIDS has impacted families since the middle ages. The first SIDS case was documented in the Bible, when a woman accidently lay on her child while co-sleeping. (Berkowitz, 2005) Infants sleeping with their parents, grandparents, and siblings were a common practice. Due to co-sleeping many infants ended up being suffocated. In The Middle Ages, 19th century and well into the first part of the 20th century, infants passing away due to co-sleeping were not a major factor. (Mahler, 2004) There were many other diseases that impacted the life of infants. For example: small pox, diphtheria, whooping cough, just to name a few. (Mahler, 2004) In 1969 the other diseases that impacted infant’s lives started becoming under control, by medication.(Mahler, 2004) With control over the other diseases of infants the disease, crib death, came into light. At this time the name was changed to Sudden Infant Death Syndrome or SIDS. Today if an infant does have a disease at death, which is found...
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...Down syndrome. It is the most common birth defect in the United States, and it’s named after the physician who first diagnosed it as a syndrome, John Langdon Down. (1) Down syndrome, in most cases, affects every cell of the body, and can cause multiple difficulties mentally and physically. Despite the hardships people born with Down syndrome have, 50% will live longer than 50 years old, and with the right support, live meaningful lives. (1) Trisomy 21 occurs when a person has 47 chromosomes rather than the normal 46. The physician can usually diagnose the condition of Down syndrome when the baby is born, and confirms the diagnosis with an extra blood...
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...Cri du chat, also known as “Cat’s Cry” syndrome or 5p- (5 p minus) syndrome occurs when there is a deletion in chromosome 5 (Genetics Home Reference). According to the Genetics Home Reference website, most cases of Cri du Chat are not inherited. The deletion occurs randomly during production of reproductive cells or in early development. People with Cri du Chat most often have no familial history of the disease. Only about ten percent of the cases of Cri du Chat are inherited from unaffected parents. Most of the time in this situation, the parent’s chromosome is rearranged. The material is not gained or lost, but is located on different parts of the chromosome. So, when the material is moved to create gametes or chromosomes in a developing...
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...at the American International School of Kuwait. I strongly believe that the negatives of designer babies outweigh the positives. Designer Babies allow parents to pick the desirable characteristics they want their child to have by genetically modify their child. Children will be genetically modified by first completing in-vitro fertilization. Then the embryo is examined by two scientists which examine the defects of the DNA. Only the wanted and disease free pieces of DNA are kept and the non-desired traits...
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...No mother wants to hear the tragic news that she is pregnant, and to find out that there is a problem that occurred. It’s at this time the mother and her spouse need to figure out their options and what they feel is right for them. One of the issues that can lead to a woman ending her pregnancy is a birth defect being found in the child. The most common birth defect that leads to abortion of the pregnancy is Trisomy 13 and Potter’s Syndrome. What Trisomy 13 is, is a birth defect on the 13th chromosome, causing intellectual defects and physical abnormalities. In most cases when a mother finds out that her fetus has this sort of condition, the doctor will discuss the options and how the end result would be if they decided to carry out the pregnancy. Most of the time once the mother gives birth the child will die immediately after birth or a few days after. Potter’s Syndrome is another one of the main birth abnormalities that cause some women to terminate pregnancies. The different defects that come along with Potter’s Syndrome are limited lung development, kidney failure, flattened nose, recessed chin, abnormal low-set ears, and so many more on the list. Even if...
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...important. Immunizations helps prevent a lot of childhood diseases and viruses. Two of the most common health problems seen in school-age children are asthma and obesity. If the three levels of prevention is applied this can help in the health of a child. Primary Prevention- Happens before the sickness occur. Like making the environment better for a child. Secondary Prevention- Avoid on-set conditions. Staying consistent with routine check-ups. Tertiary Prevention- Treating the problem after it occurs. Teaching and learning Children begin to make sense of their situations. Children become more systematic and objective Thinking Children are able to organize their knowledge and utilize it when needed and in the correct way. Brain development As the brain continues to develop in middle childhood, several behaviors that were common in early childhood can be controlled, like emotional outburst. Ongoing maturation allows children to analyze the consequences of their behaviors before engaging in them which naturally improves with age. This video shows a good understanding of what selective and automation attention is in middle childhood Special needs children There are many different disorders that a child can develop during middle childhood. Children with special needs may have mild learning disabilities or profound cognitive impairment, terminal illness or developmental delays that catch up quickly or remain entrenched, some are biological and some are unknown. When dealing...
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...to the wall of the uterine, it starts to become an embryo. That is the process of developing a human organism. After 9 weeks the embryo starts to look like a fetus or offspring. When the offspring is about 6 months of womb service, it can live outside the womb because all the main organs are developed enough (Myers, 2014). Fetal Alcohol Syndrome or FAS is caused when a pregnant mother drinks heavily. It can be a physical or cognitive disease. In some cases a child can have things wrong with their face. Fetal Alcohol Syndrome is an example of a teratogen or in other words “monster maker.” A teratogen is like a light switch for our genic codes. It’s a toxin, virus and drug that can harm your child while it’s still in the womb (Myers, 2014)....
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...Introduction Aperts syndrome is a developmental disorder of genetic origin. It is caused by a mutation of chromosome ten and is common in older dads. The disorder is due to many different reasons and is treated accordingly depending on the various symptoms. This syndrome is characterized by iconic signs and symptoms. Aperts also affects many people in many ways such as physically and intellectually. Aperts syndrome is preventable but only by abstinence. Pathophysiology, Incidence, and Diagnosis Syndactylic oxycephaly, Acrocephalo-syndactyly type 1, ACS 1, and Apert-Cruozon disease are all different names pertaining to Aperts syndrome. Aperts syndrome is a result of a mutation of the gene FGFR2 or Fibroblast Growth Factor Receptor...
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...What is Down syndrome? Down syndrome is genetic disorder that causes lifelong mental retardation, developmental delays and other problems. Down syndrome varies in severity, so development problems range from moderate to serious. Down syndrome is the most common genetic cause of severe learning disabilities in children, occurring in one in every 700 to 800 infants. Increased understanding of Down syndrome and early interventions make a big difference in the lives of both children and adults with Down syndrome. Down syndrome is also known as Trisomy 21 syndrome. Trisomy 21 is due to an extra copy of chromosomes number 21. Instead of having the normal two copies chromosomes number 21, the person with Down syndrome has three copies of chromosomes 21. Meaning normally a fertilized egg has 23 pairs of chromosomes. In most people with Down syndrome, there is an extra copy of chromosome 21. (Rogers, 2007, pg.6) The formal story began in 1866, when a physician named John Langdon Down published an essay in England in which he described a set of children with common features who were distinct from other children with mental retardation. Down was superintendent of an asylum for children with mental retardation in Surrey, England when he made the first distinction between children who were cretins (later to be found to have hypothyroidism) and what he referred to as "Mongoloids." Down based this unfortunate name on his notion that these children looked like people from Mongolia,...
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...Birth defects can be defined as structural or functional abnormalities, including metabolic disorders, which are present from birth. The term congenital disorder is considered to have the same definition; the two terms are used interchangeably.2 The eleventh revision of the classification provides an opportunity for a review of the current entry. 3. Irrespective of definition, birth defects can cause spontaneous abortions and stillbirths and are a significant but underrecognized cause of mortality and disability among infants and children under five years of age. They can be life-threatening, result in long-term disability, and negatively affect individuals, families, health-care systems and societies. BIRTH DEFECTS AND GLOBAL NEWBORN AND CHILD MORTALITY 4. Congenital disorders are a common condition. WHO estimates that some 260 000 deaths worldwide (about 7% of all neonatal deaths) were caused by congenital anomalies in 2004.3 They are most prominent as a cause of death in settings where overall...
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