WAGR Essay

My interest for the Attorney Advisor position with the United States Patent & Trademark Office (USPTO) arises from my longstanding commitment to constantly improve myself. I have always enjoyed legal research, writing, and the complexities of intellectual property. I have no doubt that my enthusiasm to research, my eagerness to learn, and my strong ability to communicate clearly, work efficiently, accurately, and quickly, will make me an invaluable asset to the USPTO. I believe these traits combined with my unique skillset, developed as a result of experiences working for the Arizona Diamondbacks of Major League Baseball (Diamondbacks), Nike Inc. (Nike), and the Arizona Attorney General’s Office, Liability Management Department (AG Office)

The complication is that many of the symptoms associated to this illness can be confused with a number of other conditions early on.

The National Organization for Rare Disorders (NORD) says that MSUD happens to males and females at the same rate. The risk of having any form of MSUD depends if your parents have this disorder or not. If both of the parents have the disorder, each child has a 25 percent chance of getting two mutated genes and getting MSUD, the child would have a 50 percent chance from getting one normal gene from each parent. The parent or parents are not able to pass on the gene to their children if they have two normal genes for MSUD. (Healthline,

Metro West Learning Academy has been a positive experience for me. It has benefited me in many ways. Metro has helped me handle stress by alleviating it. At first I didn’t want to come to Metro. I was worried about leaving all of my friends but I made some here. And the teachers here have also made it better because of how individualized the program is.

There are many forms of mental retardation. Webster’s New World Dictionary defines mental retardation as “a condition, usually congenital, characterized by subnormal intelligence” (Agnes, p404). Mental retardation can be caused by a certain birth defect due to a traumatic event during the mother’s pregnancy, or mental retardation can also be inherited. The most common inherited form of mental retardation is Fragile X Syndrome.

AS is caused by a deletion or mutation on the maternal chromosome 15, alteration in UBE3A gene, paternal uniparental disomy, translocation, or mutation in the gene that activates UBE3A gene. PWS is a deletion or mutation on the paternal chromosome 15, uniparental disomy, or translocation. The loss of the SNORD116 gene on chromosome

Wampum is traditionally beaded strings and belts which were and are used as mnemonic devices to recount historical events and agreements (Fadden & Thomas, 2006). Throughout my research a common misconception was addressed that the Haudenosaunee did not use wampum as currency, as monetary value was not established prior to contact. Though it was valued, as it was recognized to take a considerable amount of effort to make said belts (Fadden, 2015) Making wampum a key component in initiating, establishing, symbolising and recording different types of relationships between Nations. Accordingly, it is used across many different people including Anishinaabe and Haudenosaunee (Ojiig, 2015). Each nation has its own belts and teachings, for this paper we will be focusing on the Haudenosaunee teachings and traditions surrounding wampum. They can all be described as a “Cultural tape recorder” (Hill, 2016), as they capture the essence of a story and make it easier for the story to be told when the belt is there as a physical reminder. People who kept the knowledge of the

Wilms tumor is a type of cancer that starts in the kidneys. It is the most common type of kidney cancer in children. It is named after Max Wilms, a German doctor who wrote one of the first medical articles about the disease in 1899.

Williams Syndrome is a rare disease that is caused by deletion of certain genes in chromosome 7 during the formation of reproductive cells. It is known as an autosomal dominant condition because one copy of the altered chromosome 7 is all that is needed to cause Williams Syndrome. While it can be inherited from a parent who already has the disease, it can also randomly occur in anyone. It causes some medical problems along with physical abnormalities, mental capacities, and personality characteristics. This rare disease affects 1 in 7,500-10,000 people. An estimated 20,000-30,000 people in the United States currently have been diagnosed with Williams Syndrome. There is no specific gender that Williams Syndrome, it occurs equally in both of

BACKGROUND: The Wilms’ Tumor Suppressor gene (WT1) is the causative gene of Wilms tumor. WT1 mutation also causes disorders of sex development. We reported four cases of boys with external genital abnormalities and WT1 gene mutations.

The disorder affects 1 out of 40,000 newborns (Atlas Genetics). Almost 90% of patients with this disease have a parent with the disease, but the symptoms in the parent can be very different from the symptoms in the child (MedlinePlus). Waardenburg syndrome type 1 (WS1) and type 2 (WS2) are inherited as autosomal dominant traits, which means one copy of the altered gene in each cell is sufficient to cause Waardenburg syndrome (GHR). Manifestations of the disorder may not be present in individuals that inherit the altered gene for the disease. Some cases of the disorder, such as type 3 (WS3) and type 4 (WS4) have an autosomal recessive pattern of inheritance. Type 1 and type 2 of Waardenburg syndrome can also be acquired even when there is no family history of the disorder. The disorder can be caused from new genetic changes that occur spontaneously for unknown reasons. Researches indicate that new sporadic mutations for type 1 of Waardenburg syndrome may be associated with the advanced age of the father. In dominant disorders, a single copy of the gene with the disease that is either received from the mother of father will be expressed in the offspring by dominating the other normal gene, which causes the result in the appearance of the syndrome (Rare

There are so many types of diseases and disorders in this world. Some can lead to a lifetime of pain and others can lead to mortality. Robinow syndrome is a disorder that affects few people. This rare disorder is inherited to the fetus by the parents. This disorder comes in dominant form and recessive form. In dominant form you inherit the gene from only one of the parents. In recessive form you inherit the gene from both parents. In the recessive form the syndrome comes from mutations in the ROR2 gene. In the dominant form the syndrome is caused by the mutations in the WNT5A or DVL1 gene. The genes affect the development of the patient in its first years. Robinow syndrome affects both male and females. They have

Wilms’ tumor or nephroblastoma is a disease that is named after German scientist Dr. Max Wilms, who first described this disorder. Wilms’ tumor, or nephroblastoma, is the most common childhood abdominal malignancy. The median age for this diagnosis is approximately 3.5 years. Wilms’ Tumor is a malignant tumor containing metanephric blastema, epithelial derivatives and stromal (Royer-Pokora 13). Characteristic of this tumor is the presence of glomeruli and abortive tubules surrounded by a spindle cell stroma. Wilms’ tumor can originate from any site in the sympathetic nervous system and arise from neural crest cells. Most Wilms tumors are unilateral, which means they affect only one kidney. Most often there is only one tumor, but 5% to 10% of

Ultrasound is the first imaging test performed upon the suspicion of Wilms tumor because of its efficiency, safeness, and good imaging characteristics. Ultrasound uses sound waves to create the images of the organ, meaning there is no radiation involved. It gives a good view of the organs in the abdomen, as well as detecting tumor thrombus (tumor growing into the main veins coming out of the kidney). Ultrasound is also used to distinguish Wilms tumor form hydronephrosis (Eisenberg, 2016). Computed Tomography (CT scan) creates quick and detailed cross sectional images of the body’s anatomy, and is one of the most useful tests in detecting mass in the kidney.

In most cases Williams syndrome is not inherited but take place from random events during the creation and formation of the reproductive cells: eggs and sperm (gametes) (Morris, 1993). This mutation in the reproductive cells causes the disorder in the progeny of the parent’s generation despite the fact that there is only one of the seventh chromosomes affected. This dominance of the disorder shows that Williams Syndromes is autosomal dominant (Morris, 1993). To further explain this matter, Williams Syndrome is autosomal dominant because one copy of the seventh chromosome is enough to cause the disorder (Morris, 1993). It is possible as well to inherit the condition from the parent if the parent chooses to have offspring, but this is only in very rare cases (Morris