Trisomy 13 Essay, Research Paper
Trisomy 13 (Patau Syndrome)
Dr. C.J Gamble
To the Parents or Legal Guardians of Patient XC902-V42
In our extensive testing it was revealed to us that your son suffers from a genetic disorder called Trisomy 13 or Patau’s Syndrome. Trisomy 13 is a syndrome caused by an extra 13th chromosome. As you may be aware that humans have 23 chromosomes in pairs of two. In your son’s case the 13 chromosome has and extra pair. Normally it is thought that a Trisomy occurs when, at conception, either the father’s sperm or the mother’s egg contained 24 chromosomes instead of 23. When the sperm fertilized the egg the resulting cell or zygote which made up the new baby had 47 chromosomes instead of the normal 46. When it comes to chromosomes, more is not necessarily better. It is a little like adding too much of an ingredient into a cake. Even though it may look alright on the outside, inside it may not good at all. This disorder occurs in 1 out of every 20,000 live births.
It is also called Patau’s Syndrome, after Dr. Klaus Patau, who first identified the extra chromosome and published a report describing Trisomy 13 in 1960. Half of the victims of Patau’s syndrome may not survive beyond the first month and about three quarters die within six months. In essence we cannot be exactly sure as to how long your son will live, but it can be assured that he will died of this eventually.
Trisomy 13 is associated with multiple abnormalities, including severe mental defects and defects of the brain that lead to seizures, deafness, and ocular abnormalities. The eyes are small with defects in the iris. Most infants have a cleft lip and cleft palate and low-set ears. Heart disease is present in approximately 80% of affected infants. Hernias and genital abnormalities are common also.
In general the testing used to determine the presence of a genetic deformity is not susceptible to mistake. While looking for signs is only as reliable as the knowledge of the doctor, the chromosome test is highly specialized and is of course double checked. As a rule chromosome analysis is 99.9% accurate.
We are deeply saddened your misfortune and my staff and I will be by your side to the end . I hope that is of some consolation.
.
Trisomy 13 (Patau Syndrome)
Dr. C.J Gamble
To the Parents or Legal Guardians of Patient XC902-V42
In our extensive testing it was revealed to us that your son suffers from a genetic disorder called Trisomy 13 or Patau’s Syndrome. Trisomy 13 is a syndrome caused by an extra 13th chromosome. As you may be aware that humans have 23 chromosomes in pairs of two. In your son’s case the 13 chromosome has and extra pair. Normally it is thought that a Trisomy occurs when, at conception, either the father’s sperm or the mother’s egg contained 24 chromosomes instead of 23. When the sperm fertilized the egg the resulting cell or zygote which made up the new baby had 47 chromosomes instead of the normal 46. When it comes to chromosomes, more is not necessarily better. It is a little like adding too much of an ingredient into a cake. Even though it may look alright on the outside, inside it may not good at all. This disorder occurs in 1 out of every 20,000 live births.
It is also called Patau’s Syndrome, after Dr. Klaus Patau, who first identified the extra chromosome and published a report describing Trisomy 13 in 1960. Half of the victims of Patau’s syndrome may not survive beyond the first month and about three quarters die within six months. In essence we cannot be exactly sure as to how long your son will live, but it can be assured that he will died of this eventually.
Trisomy 13 is associated with multiple abnormalities, including severe mental defects and defects of the brain that lead to seizures, deafness, and ocular abnormalities. The eyes are small with defects in the iris. Most infants have a cleft lip and cleft palate and low-set ears. Heart disease is present in approximately 80% of affected infants. Hernias and genital abnormalities are common also.
In general the testing used to determine the presence of a genetic deformity is not susceptible to mistake. While looking for signs is only as reliable as the knowledge of the doctor, the chromosome test is highly specialized and is of course double checked. As a rule chromosome analysis is 99.9% accurate.
We are deeply saddened your misfortune and my staff and I will be by your side to the end . I hope that is of some consolation.
.
Trisomy 13 (Patau Syndrome)
Dr. C.J Gamble
To the Parents or Legal Guardians of Patient XC902-V42
In our extensive testing it was revealed to us that your son suffers from a genetic disorder called Trisomy 13 or Patau’s Syndrome. Trisomy 13 is a syndrome caused by an extra 13th chromosome. As you may be aware that humans have 23 chromosomes in pairs of two. In your son’s case the 13 chromosome has and extra pair. Normally it is thought that a Trisomy occurs when, at conception, either the father’s sperm or the mother’s egg contained 24 chromosomes instead of 23. When the sperm fertilized the egg the resulting cell or zygote which made up the new baby had 47 chromosomes instead of the normal 46. When it comes to chromosomes, more is not necessarily better. It is a little like adding too much of an ingredient into a cake. Even though it may look alright on the outside, inside it may not good at all. This disorder occurs in 1 out of every 20,000 live births.
It is also called Patau’s Syndrome, after Dr. Klaus Patau, who first identified the extra chromosome and published a report describing Trisomy 13 in 1960. Half of the victims of Patau’s syndrome may not survive beyond the first month and about three quarters die within six months. In essence we cannot be exactly sure as to how long your son will live, but it can be assured that he will died of this eventually.
Trisomy 13 is associated with multiple abnormalities, including severe mental defects and defects of the brain that lead to seizures, deafness, and ocular abnormalities. The eyes are small with defects in the iris. Most infants have a cleft lip and cleft palate and low-set ears. Heart disease is present in approximately 80% of affected infants. Hernias and genital abnormalities are common also.
In general the testing used to determine the presence of a genetic deformity is not susceptible to mistake. While looking for signs is only as reliable as the knowledge of the doctor, the chromosome test is highly specialized and is of course double checked. As a rule chromosome analysis is 99.9% accurate.
We are deeply saddened your misfortune and my staff and I will be by your side to the end . I hope that is of some consolation.
.
Другие работы по теме:
Kids W Disabilities Ds Essay Research Paper
Down syndrome affects many people in this world. Not only does it affect the person diagnosed as Downs, but it also affects their family and everyone around them. There are physical characteristics that help you identify somebody with Downs. There are also some health concerns that you need to worry about.
Charcot Marie Tooth Disease Essay Research Paper
Charcot-Marie-Tooth Disorder Charcot-Marie-Tooth Disorder (CMT) is the most common type of hereditary motor and sensory neuropathy (HMSN), occurring in one of every 2500 births. The mean age of onset of clinical symptoms is 12.2 7.3 years. Severity of the disorder varies among the individual and among the subtypes of CMT.
Romeo An Juliet Essay Research Paper hi
Romeo An Juliet Essay, Research Paper hi i need an essay about a character in romeo and juliet that demonsrtated maturity. in a well developed multi pagraph essay and say why you think the character’s maturity was greater than the other characters in the play.
Down Syndrome And Spina Bifida
– Cause, Effects And Treatment Essay, Research Paper Many individuals are born with defects due to genetic factors. Some such defects occur because the child inherits a defective gene, or genes from the parents. Others are caused through mutations- spontaneous changes that occur to a gene or chromosome.
Genetic Disorders Essay Research Paper Chris Grounds
Genetic Disorders Essay, Research Paper Chris Grounds CCS Biology II 10/3/00 Earth?s inhabitants have populated all of the regions of the world, discovered places never dreamed of, and have advanced beyond normal understanding, while man can still be conquered by an object which is immeasurably small.
Downs Syndrome Essay Research Paper IntroductionIn the
Downs Syndrome Essay, Research Paper IntroductionIn the United States about one in every 1000 live births is a child with Downs Syndrome. Downs Syndrome affects all races and genders. It is caused by extra genetic material on the twenty-first chromosome. There are three different types of Downs Syndrome known to man today.
Oh Really Essay Research Paper Oh Reallyyou
Oh Really? Essay, Research Paper Oh Really, you think i am a lark, the dogs they run and bark, but when i say to them, shut up shut up shut up, you say to be nice to them,
Down S Syndrome Essay Research Paper I
Down S Syndrome Essay, Research Paper I. What I knew I remember looking at my cousin Ricky and wondering why he looked so different. He was the only one in a family of dark skinned Hispanics who was stark white. He had blond hair, beady blue eyes, a stocky body frame and a laugh that echoed throughout the mountains of Tucson.
Cri Du Chat Syndrome Essay Research Paper
Cri Du Chat Syndrome (Cry of the Cat) By Chase Kuntz The Cri du Chat syndrome is the result of the deletion of segment 5p15.2 in the short arm of chromosome number five. No one is quite sure on how this deletion occurs, or even why it occurs. This deletion leads to deformities and mental retardation in the child.
Shane Essay Research Paper Sometimes I need
Shane Essay, Research Paper Sometimes, I need you more than I need air And sometimes I miss you more than I will forever, never forget the times that we have shaared. The are priceless
Poem Belong Essay Research Paper Where I
Poem: Belong Essay, Research Paper Where I belong I am weak, I am strong I will fit where I belong don’t know where it is for now but it will come, if I allow tomorrow, I start a brand new day
Down Syndrome Essay Research Paper Down Syndrome
Down Syndrome Essay, Research Paper Down Syndrome or Trisomy 21 as it is also commonly known, is a genetic condition that for many years has been shrouded in fear, darkness & shame. There is absoultely nothing to fear, and there never should be any feelings of shame, it is not the persons fault. The only darkness associated with down syndrome is the ignorance many people have towards it.
TRIDOMY 18 Essay Research Paper TRISOMY 18
TRIDOMY 18 Essay, Research Paper TRISOMY 18 SYNDROME DEFINITION: A chromosomal disorder resulting in a syndrome characterized by specific (small) dysmorphic features and organ malformations.
Meiosis Essay Research Paper State that meiosis
Meiosis Essay, Research Paper State that meiosis is a reduction division in terms of diploid and haploid numbers of chromosomes Outline the process of meiosis including pairing of chromosomes followed by
Him Essay Research Paper I think about
Him Essay, Research Paper I think about him day and night The though won’t go away And, oh, how I would hold him tight every second of the day He is perfect, that is true, not an average me or you
Poem She Sat Essay Research Paper She
Poem: She Sat Essay, Research Paper She sat… helpless in her room praying to whatever god there may be to let her call to him. could god ignore such a painful cry?
Trisomy 21
“Down Syndrome” Essay, Research Paper Trisomy 21 is caused, as the name suggests, by the triplication of the 21st chromosome. Genes which, simplified, contain the blueprints for our cellular structure, are grouped along rod-like structures called chromosomes. Normally, the nucleus of each cell contains 23 pairs of chromosomes, half of which are inherited from each parent.
Chromosome Probes Essay Research Paper Chromosome ProbesSensitive
Chromosome Probes Essay, Research Paper Chromosome Probes Sensitive chromosome probes recently discovered by a University of Toronto geneticist will make it easier to detect certain types of genetic and prenatal diseases, as well as being used to determine paternity and provide forensic evidence in criminal
Ode To Boys Essay Research Paper We
Ode To Boys Essay, Research Paper We like them But do they like us The ones we do never fuss They don’t stop in And we wonder why We stress, we bitch We sometimes cry
ChromoA Essay Research Paper Chromosome Probes at
Chromo(A) Essay, Research Paper Chromosome Probes at the University of Toronto Sensitive chromosome probes recently discovered by aUniversity of Toronto geneticist will make it easierto detect certain types of genetic and prenataldiseases, as well as being used to determine paternityand provide forensic evidence in criminal cases.
Life Is Like Essay Research Paper Life
Life Is Like Essay, Research Paper Life is like a car. When it?s new, it usually works all right. As time drives by, it breaks down and needs repairs. Life is like a leaf. In its youth, it
Dare Essay Essay Research Paper What DARE
Dare Essay Essay, Research Paper What D.A.R.E Means To Me Dare has prepared me to say no to drugs in eight different ways. If anyone asks me to do drugs I will know what to do, such as- just ignoring the person or just
The Playground Essay Research Paper I have
The Playground Essay, Research Paper I have a friend I used to know who had a playground where we would go The times we had are fresh in my mind but they are from another time
Down Syndrome Report Essay Research Paper Down
Down Syndrome Report Essay, Research Paper Down Syndrome Report by: SCHOOL SUX The chromosomal abnormality involved in most cases of Down syndrome is trisomy-21, or the presence of three copies of the 21st chromosome. As a result,
Down Syndrome 3 Essay Research Paper Down
Down Syndrome 3 Essay, Research Paper Down Syndrome Down Syndrome is a chromosomal disorder. It occurs in about 1 of every 800 births. People with Down syndrome may have mild to severe learning disabilities. Physical symptoms include a small skull, extra folds of skin under the eyes, and a protruding tongue.