Genetic disorders are a topic in biology that can not be avoided. The fact is that genetic disorders can happen in humans, plants or animal. No one and nothing is safe from a genetic disorder. A genetic disorder can appear in the first years off life, or can appear much later in life when least expected. A basic principal of biology states that the behavior of chromosomes during the meiosis process can account for genetic inheritance patterns. There are many reasons for genetic disorders.
To start it is important to understand what a genetic disorder is. It is a mutation in the genetic material of a person. The mutant gene is transmitted thru birth. These genetic mutations can create serious complications and even death.
It is important to understand how people get certain traits and genes. A person receives one set of chromosomes and genes from each person. That means each person inherits the traits. One gene may be more influential then another in developing specific traits. The more powerful gene is called the dominant gene and the less powerful is the recessive. A variation of a gene and the trait it controls, such as the color of ones eyes or hair is called in allele.
Most diseases have genetic disorders. A diseases springs from genetics that are passed along from the parents. So called genetic diseases can be classified in 3 ways single gene defects, chromosomal disorders and multi factorial. 1 in 200 births have single gene defects. There are over 6000 different known single gene disorders. These kind of disorders are characterized by the way they are carried thru a family.
In dominant inheritance the child of a carrier has a fifty percent chance of inheriting the gene. The parents of the children with genetic disorders are definitely carriers. While in recessive inheritance the parents do not necessarily have the gene. The chances vary with each generation of recessive genes. It also depends on the sex of the baby.
Recessive traits can only be expressed if both of the genes have the same mutation. Without both parents having the gene it is impossible for the disease to show up in their child. Although the child can have the recessive trait. T...
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... can be cured some can be prevented and suppressed. Many people live long and productive lives with these diseases.
The diseases that are listed in the paper are just but a little taste of the many diseases that can occur in a child or an adult. Inheritance plays a big part of how genetic diseases occur in a person.
As a rule there are sporadic times when abnormalities occur in the gametes. Therefore it is possible for only one person in a huge family to have a disorder. When diagnosed with certain disease it is very obvious. Yet it might take time for the afflicted person to have symptoms.
It is important for parents who are expecting children to try and map out their family history of diseases. That way they can see if either of them might have 1 dominant or recessive gene. It is possible for a family to go many generation without any of the genetic disorders showing up.
Understanding the disorders and how they happen can help parents to prevent having children who will suffer for many years. There is many different ways for a person to inherit a mutated gene.
There are other poetry such as traditional poetry that are romantic and soothing is poems that I adore. The sensation of love brings me happiness and the desire to be a better person to others. This universe is occupied with lovely people who spread their adoration with everybody around them, increasing the happiness in everybody’s mood. If you live with misery and repentance, then it’ll be embedded in you for the rest of your life until you’ll never be able to find your happiness. This poem is spoken in second person point in view, this certain person is telling his/her readers to do the virtuous thing so you won’t have to face consequences. He/she also shows the guilt you feel for committing a debauched crime, could be a lesson learn from the individual. This poem contains 3 stanzas, it’s not a sonnet, and it’s literal. This poem don’t have a pattern of rhyming, so everything is unswerving and could easily
...hich inherited traits, such as those for genetic disease, can be tracked over generations. Throughout out the course of human development, scientists will continue to find new new ways to help the human race through the discovery of the human gene inside of each of us, its uses, as well as complications, that can help the survival of our species.
In the book it says "They can spend a whole lifetime worrying whether they 're carriers, and then we come along and offer them a test. Recessives and X-linked. Look what they 're doing with fragile-X nowadays. And cystic fibrosis. Just imagine the commercial possibilities if you can design and patent a probe for something like Gaucher 's disease...(69)" Recessive traits is the phenotype is seen only a homozygous recessive genotype for the traits of the interest is present. The booked talked about two of three diseases that are most common in the Ashkenazi Jewish population. The first one is Cystic fibrosis which is an inherited life-threatening disorder that effects the lungs and the digestive system. The other one mention in the book that wasn’t mention in class was Gaucher 's disease. Gaucher 's disease is a build up of fatty substances in your organs, usually in you spleen and liver. Which causes them to become bigger affecting their function. The last one that we learned in class was Tay-Sachs disease, which is a rare inherited disorder that destroys nerve cells in the brain and spinal
· genetics: occasionally the disease has a tendency to run in certain families (inherited or genetic predisposition), but this is not common.
Genetic disorders can be caused by many of the 46 chromosomes in human cells. This specific disorder is linked to a mutation in the long arm of the X, or 23rd chromosome. The mutation is recessive, meaning a normal X chromosome can hide it. Females have two X chromosomes allowing them to hide the mutated recessive one, making them a carrier of the gene, while males only have one X chromosome, meaning that they are unable to hide the mutation and they become effected by the disease. Therefore if a male carries the gene, he is affected because he has no way of dominating the recessive gene, but if a female carries it, she is only a carrier and has a 50/50 chance of passing it on to her baby. This may seem like a high probability however, only one in every fifty thousand male births will have this immunodeficiency disease.
A genetic disorder is a sickness caused by one or many abnormalities or absentees in the genes or chromosomes. One interesting genetic disorder such as cancer, are found genetic but, can also be caused and affected by many by environmental factors such as being exposed to asbestos which may increase the risk of lung cancer and many other cancers. While on the other hand most disorders like Williams Syndrome are genetic and are primarily rare and only affect a limited amount of people about one in every several thousand. Because it is a genetic disorder that is estimated between 1 in 10,000 people worldwide, primarily caused by a micro-deletion on the seventh chromosome is what indicates the disorder being Williams Syndrome.
Turner’s syndrome is a genetic conditions that affects the female’s sex chromosome. In (http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001417/) Turner’s syndrome occurs when cells are missing all or part of an X chromosome. It’s common of the female patient to only have one X chromosome. Although, some individuals may have two X chromosomes but one is defective. It is thought that an estimated 1 out of 2000-2500 females suffer from this genetic condition worldwide but it’s usually females with this condition don’t survive their birth. Due to this abnormality, the genes that is defective “affect the growth and sexual development of the female” (http://learn.genetics.utah.edu/content/disorders/whataregd/turner/). However other disabilities and delays do occur even though these traits can vary case by case.
It is important to note that genes themselves do not cause disease genetic disorders are caused by mutations that make a gene function improperly. For example, when people say that someone has the cystic fibrosis gene, they are usually referring to a mutated version of the Cystic Fibrosis Transmembrane Conductance Regulator gene, which causes the disease. All people, including those without cystic fibrosis, have a version of the Cystic Fibrosis Transmembrane Conductance Regulator gene.
Bulimia Nervous, as defined by the National Eating Disorders Association, is a serious, potentially life-threatening eating disorder characterized by a cycle of bingeing and compensatory behaviors such as self-induced vomiting. It affects 1 - 2 percent of the adolescents and young adults. About 80 percent of the people it affects are female. Many people struggling with Bulimia Nervous also struggle with depression and social phobias. The disorder is often shortened from Bulimia Nervosa to just Bulimia. Many people do not understand the severity of the Eating Disorder (ED) at hand. Many people will brush it off as if the sufferer is just wanting attention. What many people do not understand is that, the sufferer has a warped body image and they are suffering mentally and physically with this disorder. Having Bulimia, you binge, and eat your desired food, then you realize the mass of intake and you purge, either through vomiting, exercise, or laxatives. This vicious cycle is a sensation and becomes very addictive which leads the person to the severe disorder of Bulimia Ne...
The desire to have a "normal" child is held by every parent and only now are we beginning to have the ability to select for that child. In preparation to receiving genetic testing, the parents are required to meet with a genetic counselor. A detailed description of the testing methods are reviewed with the couple as well as the risks which are involved with each. Upon an understanding of the procedures, the counselor discusses the many possible outcomes which could be the result of the diagnosis. Finally, before any tests are performed, anxieties from either of the parents are addressed as well as the psychological well-being of the parents.
For almost all types of Albinism both parents or mates must carry an albinism gene in order for their child to have albinism. Because the body has two sets of genes, a person may have normal pigmentation but carry the albinism gene. If a person has one normal gene and one albinism gene that is still enough to pass the disease on to their children. Even if both parents have the albinism gene it does not mean they have the sickness. The baby will have a one out of four chance of getting the disease. This is inherited by autosomal recessive inheritance.
The past two decades have overwhelmed the human experience with technology, along with all its distractions. The direct relationship between the mind and the body’s ability to adjust from these distractions can be extremely difficult .Further research has shown that it has become an addiction for many. Technology has significantly improved our lives as a whole through experiences such as Global Positioning System (GPS), cell phones and social networking allowing us to communicate with different people around the world. These technologies make our daily lives easier and more efficient. However, this also discusses the effects of technology on various aspects of our everyday personal experiences both with each other and with the world around us. On the other hand technologies such as cell phones have become a problem in getting students to focus in class and distracting drivers and thus, resulting in vehicle accidents. Technology is beneficial, but can also become an inescapable distraction in our lives. It is important to view technology as having the ability to make our lives better or worse, yet also as having the ability to change our personal lives and behavioral patterns.
The genetic defect that causes albinism in other types of albinism is unknown, but it is speculated that it involves other enzymes used to make pigment. Albinism is passed from parents to their children through genes. For nearly all types of albinism, both parents must carry an albinism gene to have a child with albinism. Parents may have normal pigmentation, but still carry the gene. When both parents carry the gene, and neither parent has albinism, there is a one in four chance at each pregnancy that the baby will be born with albinism.
GSD I is an inherited autosomal recessive disorder with the incidence being 1 in 100,000. Parents may be heterozygote carriers, making them asymptomatic, however they have a 25% chance of having a child that is affected by GSD I. Prenatal diagnosis can be made by completing a liver biopsy at 18-22 weeks but no fetal treatments are currently available and standard newborn screening tests are not able to detect GSD I.
Most diseases are caused by a type of genetic component. Many of the diseases that have been caused by gene mutations are undiagnosed. These remain undiagnosed because the disease is so rare that the doctor does not know how to diagnose the patient. Many sy...