Neonatal Abstinence Syndrome for a baby. Even though there is no evidence that nicotine‚ amphetamines‚ cocaine and marijuana causes Neonatal Abstinence Syndrome but they may contribute to the severity of the baby’s symptoms. "Neonatal Abstinence Syndrome." MedlinePlus Medical Encyclopedia. N.p.‚ 3 Nov. 2015. Web. 01 Feb. 2017. . There are a variety of drugs a mother can take to give the child Neonatal Abstinence Syndrome. A child that is born with Neonatal Abstinence Syndrome will show a variety
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Speech Topic: Asperger’s Syndrome General Purpose: To Inform Specific Purpose: To inform my audience about a mild variant of Autism called Asperger’s Syndrome. Thesis: Asperger’s Syndrome is a fairly common‚ but it is still widely misunderstood because of its unique characteristics and connotations. I. Introduction A Attention Getter: “In the popular sitcom The Big Bang Theory‚ the character Shelton is clearly suffering from Asperger’s Syndrome‚” says writer Paul Collins
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Genetic Project: Down Syndrome What is Down Syndrome? Down Syndrome is a chromosomal disorder where a child is born with an extra partial or full chromosome 21‚ thus leading to the over-expression of many genes present on this extra chromosome. Therefore‚ it is neither dominant nor recessive. Down Syndrome affects about 1 in 700 babies born‚ making it one of the most common genetic birth defects in the United States. There are actually 3 different types of Down Syndrome‚ Trisomy 21 (Nondisjunction)
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Jacobs Syndrome Jacobs Syndrome‚ also known as XYY Syndrome‚ is a rare genetic disorder which affects males due to an extra Y chromosome. Males with this syndrome are sometimes called super males. Klinefelter’s syndrome with an extra X-chromosome (47‚XXY) and Turner’s syndrome with lack of X-chromosome material (45‚X) have been named after the physicians who first described the syndromes in 1942 and 1937. When Sandberg and co-wokers in 1961 found the chromosome constitution 47‚XYY‚ the name became
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Aarskog Syndrome Description Aarskog syndrome (also known as Aarskog–Scott syndrome‚ faciodigitogenital syndrome‚ shawl scrotum syndrome and faciogenital dysplasia) is a rare autosomal X-linked inherited disorder that affects a person’s height‚ muscles‚ skeleton‚ genitals‚ and appearance of the face. It mostly affects at birth and the symptoms usually become apparent by the age of 3years. Unfortunately‚ Aarskog syndrome is a lifelong condition without a cure. Some people with Aarskog syndrome are born
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Prognosis The prognosis for Williams Syndrome is not bright in some areas and bright in others. Since there is no cure for this genetic disorder‚ treatment in no way can change the prognosis unless it is to alleviate a symptom of this disorder. Cardiovascular symptoms aside‚ individuals suffering from this disorder can live a healthy and long life if properly cared for and nurtured‚ but this is very rare. There are several ways to discuss the prognosis for this disorder and they are: life expectancy
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Rett Syndrome: Important to Diagnose Imagine this‚ you are enjoying the Christmas holiday at your grandparents with your aunts‚ uncles‚ and cousins. You think nothing of it because it is a completely normal thing to do. This is the first year all of my cousins were together in about three years. I introduced my boyfriend‚ Devin‚ to my other cousins he hadn’t met yet. As we were talking‚ I grabbed a plate of snacks when my five year old cousin walks up to me. She did not say anything just stared
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Countless people around the world suffer from Carpal Tunnel Syndrome. Or in other words‚ a numbness and tingling in the hand and arm caused by a pinched nerve in the wrist. Many citizens believe that the issue of Carpal Tunnel Syndrom may be a personal problem. Although‚ in reality it is a major political issue. Many workers miss days at a time because of the pain that working brings. “The median nerve runs from your forearm through a passageway in your wrist (carpal tunnel) to your hand. It provides
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Townes-Brocks syndrome is an autosomal dominant inheritance syndrome that is caused by mutations in SALL1‚ which is located on 16q12.1 and whose gene product is a zinc finger protein that acts as a transcription factor gene (Kohlhase 2016). This syndrome is often caused by a variety of mutations such as nonsense‚ frame-shift‚ deletions‚ duplications and insertions. More severe cases have been related to a dominant negative or positive effect of a truncated protein (Stevens and May 2016). The prevalence
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Sotos Syndrome‚ Pediatric Sotos syndrome is a disorder that results in increased growth during childhood‚ clumsiness‚ and delay in mental development. Over time‚ many children with Sotos syndrome catch up in mental development. Physical growth eventually slows down. By puberty‚ most children with Sotos syndrome are similar in size to other children their age. Most children with this disorder grow up and lead normal lives. CAUSES The cause of Sotos syndrome is a mutation in a gene. The gene
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