DNA is Everywhere

Understanding DNA can take a lot of studying and confusion to even get the general idea of the concept. The structure of DNA is very complicated and complex to understand, but researchers James Watson, Francis Crick, Maurice Wilkins, and Rosalind Franklin all developed the idea of the DNA structure in 1953. Deoxyribonucleic Acid is found in the nucleus of the cell. It is a double stranded molecule that contains the genetic code and is the main component of chromosomes. DNA is the blueprint of organisms. Nucleotides are the basic unit of DNA and they are made up of sugar, phosphate, and one of the four basis including adenine,

DNA is the genetic material that makes up the characteristics of all living organisms. While all human DNA is very similar in nature, there is just enough differences in

Turner syndrome results in a monosomie of chromosome X and is the only viable monosomie known. One in every 5,000 newborns can inherit this disease. The mental abilities are not affected, although they are usually sterile owing to underdeveloped sex

Turner Syndrome is a disorder that affects one in every two thousand girls. Usually girls are born with only one X chromosomes. Some are born with an extra chromosome, or sometimes even half of one is missing which causes Turner Syndrome.

Gonadal Dysgenesis, also known as turner syndrome, is a rare medical disorder that affects 1 in every 2,500 girls (kidshealth). It is a chromosomal that occurs when one of the two X chromosomes found in females are missing or is incomplete. This condition only affects females. Although researches don’t know exactly what cause turner syndrome, they do know that it’s a problem with a female chromosome. Females who are born with Tuner Syndrome are short in height and effects their sexual development and the ability to have children. Other features of this condition that can vary among women who have turner syndrome include: extra skin on the neck, heart defects, puffiness or swelling on the hands and feet, and/or kidney failure.

About 10% of all miscarriages have this disease to blame. Turner syndrome happens when a female’s X chromosome has both X’s in one cell, but not others (called Mosaic Turner Syndrome), or entirely missing (called Monosomy). It can also happen when instead of two X chromosomes, there’s one X and a small part of a Y chromosome. The girl will still develop as a female, however. All of these forms of Turner Syndrome can result in physical problems like heart or kidney defects, a shorter than normal stature, a failure to start puberty, and infertility, and mental problems like learning disabilities and social adjustment problems, to name just a few symptoms.

Turner Syndrome is a sex chromosome disease caused by complete or partial monosomy which effects on average 1 in 2500 females (Porth, 2005). Doctor Henry Turner, an endocrinologist, discovered Turner Syndrome in 1938 (Hayden, 2013). This disease is believed to be responsible for up to 10% of spontaneous miscarriages, and many Turner Syndrome pregnancies are electively aborted (Hayden, 2013). Turner Syndrome only affects females; however, this disease can affect all ethnicities. Patients who have Turner Syndrome typically exhibit various signs, including short stature, lymphedema, low hair-line, and webbed neck. Women with Turner Syndrome typically have a narrow maxilla and a high-arched palate, and they may also have a bite abnormality.

The turner syndrome can only be effected by girls, one of the main symptoms is that the girl who has it tends to be shorter..Boys are not able to get the turner syndrome (only girls). Doctors don’t know exactly what the turner syndrome is they just know that it has to do with a girls chromosomes. Most girls with turner syndrome are

DNA, Deoxyribonucleic Acid, is the basic structure for all life, it is the blueprint, the instruction manual, on how to build a living organism. DNA is made up of four nitrogen bases, adenine, thymine, cytosine, and guanine which are connected by sugar-phosphate bonds. Through a process called Protein Synthesis, the nitrogen bases are the code for the creation of amino acids. Essentially, DNA makes amino acids, amino acids make proteins, proteins make organisms. This process has been taking place for much longer than scientists have been able to document. Those scientists are called geneticists and their field is genetics.

Turner syndrome is not a walk in the park. The medical condition comes with major complications that researchers are working on finding other ways to help these girls live with the medical condition better. Turner syndrome affects about 1 in 3000 females. Monosomy, can happen in the zygote stage and leave behind long term complications, also they have symptoms that are noticeable, and treatments that help the girl develop to live longer due to new developments and reproduce.

Turner’s syndrome is a condition that effects 1 in 2,500 newborn girls (Bondy, C.A. 2009). There are many names for this condition including 45 X, TS, Ullrich-Turner syndrome, and Turner syndrome. While females usually have two X chromosomes, these girls are born with only one X chromosome or the second X is altered. While some of the babies make it through full term, some who have this condition are prone to unexpectedly aborting. Diagnosis of the missing or altered chromosome could happen during development in the womb or any time after birth. Heart defects can be related to TS along with physical abnormalities that catch the eye of doctors. Not all girls with this condition are prone to having learning disabilities, but it varies between individuals.

DNA is a molecule that converts an organisms genetic blueprint. Every person’s body has the same DNA. Apportion of your DNA is located in the cells nucleus, but a small portion of DNA can also be found in the mitochondria. The DNA structure is very important because it defines who we are and how we look. The information in DNA is stored as a code made up of four chemical bases: adenine, guanine, cytosine, and thymine. The nucleotides are joined to one another in a chain by covalent bonds between the sugar. human DNA have 3 billion bases, and more than 99 percent of those bases are the same as in all the humans in the world. DNA is a nucleic acid; proteins and carbohydrates, nucleic acids compose the three major macromolecules for all known

Turner syndrome is a chromosomal condition that affects development in females, which is also known as 45, X Syndrome; this disease affects the X sex chromosome, or the Y chromosome that determines the male features. If the whole other sex chromosome is missing the sex of the child will invariably be female, that is the classic Turner's syndrome. Mosaic Turner syndrome is where the female has one complete sex chromosome, and the other is partially missing. By the age of five, they start to develop a short stature, and a early loss of ovarian function; some girls and women will have more symptoms than others. In some cases, a diagnosis of Turner syndrome is made when a girl normally approaches puberty (Genetics Education, 2018). Although they

Turner syndrome is caused by the partial or complete loss of one X chromosome in females. Turner syndrome can only happen

What is Turner Syndrome? Turner Syndrome was named after Dr. Henry Turner who discovered it in 1938, but also referred to as Ullrich-Turner, Bonnevie-Ullrich-Turner, and Gonadal Dysgenesis. This syndrome occurs in 1 out of 200,000 females. Making it a rare syndrome that only 70,000 people in the whole world has. Turner syndrome is a lifelong condition. Most people live long and healthy lives, yet some are susceptible to numerous chronic conditions. Genes are passed on to a child from each parent, in structures called chromosomes. You have 23 pairs of chromosomes in each cell of your body. Each chromosome contains thousands of genes. Our genes determine how our body functions, what we look like and sometimes what diseases we will get. A female